| Device | CLASS II | Model Number SM-40HF-B-d-c; 40KW Canon Ready, Mobile X-ray system recalled | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | 266122 Salem Sump" Stomach Tube, Dual Lumen recalled | Cardinal Health 200 | Device Malfunction | Nationwide |
| Device | CLASS III | One Step Sterile Lancet for Single Use (3 sizes) recalled | Home Health US | Other | Nationwide |
| Device | CLASS II | HeartSine Pad-Pak recalled by HeartSine Technologies | HeartSine Technologies | Other | Nationwide |
| Device | CLASS II | BD Phoenix M50 Instrument, labeled as the following recalled | Becton Dickinson | Other | Nationwide |
| Device | CLASS II | Optima NX; dual-head nuclear medicine gamma camera designed recalled | GE Medical Systems Israel Functional Imaging | Other | |
| Device | CLASS II | Model SM-32HF-Batt; 32KW Analog, Mobile X-ray system recalled by Sedecal | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | Model Number SM-40HF-B-d-c; 40KW70CDEMO.005, Mobile X-ray system recalled | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | BD MAX System, for in vitro diagnostic (IVD) use recalled | Becton Dickinson | Other | Nationwide |
| Device | CLASS II | Model Number 40KWFX, Mobile X-ray system recalled by Sedecal | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | Model Number SM-40HF-B-d-c; 40KW 50G, Mobile X-ray system recalled | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | Shanghai United Imaging Healthcare Co., Ltd recalled by UIH Technologies | UIH Technologies | Other | TX |
| Device | CLASS II | Maxicam; dual-head nuclear medicine gamma camera designed recalled | GE Medical Systems Israel Functional Imaging | Other | |
| Device | CLASS II | Model Number SM-40HF-B-d-c; 40KW 55C/60C, Mobile X-ray system recalled | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | Model Number SM-40HF-Batt; 40KW Analog, Mobile X-ray system recalled | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | Low Prof Lckng Screw, F/im Nail / L / Xl25/ Ster recalled | Synthes (USA) Products | Packaging Defects | Nationwide |
| Device | CLASS II | Model Number 40KWFXPLUS, Mobile X-ray system recalled by Sedecal | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | Model Number SM-40HF-B-d-c; 40KW Canon Ready.005 recalled by Sedecal | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | DxC 500i Clinical Analyzer Modules recalled by Beckman Coulter | Beckman Coulter | Potency & Assay | Nationwide |
| Device | CLASS II | Model Number SM-40HF-B-d-c; 40KW 70C EN, Mobile X-ray system recalled | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | Model Number SM-40HF-B-d-c; 40KW 50C, Mobile X-ray system recalled | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | ZipTight, Acute AC Joint Implant, Single Ziploop recalled by Biomet | Biomet | Other | IN |
| Device | CLASS II | Shanghai United Imaging Healthcare Co., Ltd recalled by UIH Technologies | UIH Technologies | Other | TX |
| Device | CLASS II | Elscint Cardial recalled by Ge Medical Systems Israel | GE Medical Systems Israel Functional Imaging | Other | |
| Device | CLASS II | SED URS LP, Mobile X-ray system recalled by Sedecal | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | Model Number SM-40HF-B-d-c; 40KW 50G, Mobile X-ray system recalled | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | Artegraft¿ Collagen Vascular Graft recalled by LeMaitre Vascular | LeMaitre Vascular | Packaging Defects | AR |
| Device | CLASS II | Model Number SM-40HF-B-d-c; 40KW 70C Ready, Mobile X-ray system recalled | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | Model Number 40KWFXPLUS-710CW, Mobile X-ray system recalled by Sedecal | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | Model Number SM-40HF-B-d-c; 40KW 55C, Mobile X-ray system recalled | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | Model SM-40HF-B-d-c; 40KW 70C, Mobile X-ray system recalled by Sedecal | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | Model Number SM-40HF-B-d-c; 40KW 55C, Mobile X-ray system recalled | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | BD Bactec Blood Culture System, labeled as the following recalled | Becton Dickinson | Packaging Defects | Nationwide |
| Device | CLASS II | Easy Moving Plus recalled by Sedecal | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | 8888264911E ENFit" Salem Sump" PVC Tube 8888264929E ENFit" recalled | Cardinal Health 200 | Device Malfunction | Nationwide |
| Device | CLASS II | BD Veritor Connect recalled by Becton Dickinson & | Becton Dickinson | Device Malfunction | Nationwide |
| Device | CLASS II | Model Number SM-40HF-B-d-c; 40KW 55G, Mobile X-ray system recalled | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | Shanghai United Imaging Healthcare Co., Ltd recalled by UIH Technologies | UIH Technologies | Other | TX |
| Device | CLASS II | Model Number 40KWFXPLUS.002, Mobile X-ray system recalled by Sedecal | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | Shanghai United Imaging Healthcare Co., Ltd recalled by UIH Technologies | UIH Technologies | Other | TX |
| Device | CLASS I | Hemodialysis Bloodlines Streamline Bloodline Set For Dialog recalled | B Braun Medical | Device Malfunction | Nationwide |
| Device | CLASS II | Model Number SM-40HF-B-d-c; 40KW 80C, Mobile X-ray system recalled | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | Millenium MPS recalled by Ge Medical Systems Israel | GE Medical Systems Israel Functional Imaging | Other | |
| Device | CLASS II | 266197 Salem Sump" Anti-Reflux Valve CE Marked recalled | Cardinal Health 200 | Device Malfunction | Nationwide |
| Device | CLASS II | Elscint Varicam recalled by Ge Medical Systems Israel | GE Medical Systems Israel Functional Imaging | Other | |
| Device | CLASS II | Model Number 40KWFXPLUS.005, Mobile X-ray system recalled by Sedecal | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | Model Number 40KWMOBILE3.899, Mobile X-ray system recalled by Sedecal | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | Elscint SPX4 recalled by Ge Medical Systems Israel | GE Medical Systems Israel Functional Imaging | Other | |
| Device | CLASS II | Mobile Digital Diagnostic X-Ray Systems recalled by Sedecal | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | BD Bactec Blood Culture System, labeled as the following recalled | Becton Dickinson | Other | Nationwide |
| Device | CLASS II | DxI 9000 Access Immunoassay Analyzer recalled by Beckman Coulter | Beckman Coulter | Potency & Assay | Nationwide |
| Device | CLASS II | GE Healthcare Carescape Central Station (CSCS) V3 MAS800 Desktop recalled | Wipro GE Healthcare Private | Device Malfunction | |
| Device | CLASS II | Radpro Mobile, Mobile X-ray system recalled by Sedecal | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | Sopha Medical Vision (Smv) DSXi/Dst-XLi,/ Dst-xl/ DSTi recalled | GE Medical Systems Israel Functional Imaging | Other | |
| Device | CLASS II | SM_40HF_BDC, Mobile X-ray system recalled by Sedecal | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | Model Number SM-40HF-B-d-c; 40KW 55G/60G, Mobile X-ray system recalled | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | Low Prof Lckng Screw, F/im Nail / L / Xl25/ Ster recalled | Synthes (USA) Products | Packaging Defects | Nationwide |
| Device | CLASS II | Elscint Helix recalled by Ge Medical Systems Israel | GE Medical Systems Israel Functional Imaging | Other | |
| Device | CLASS II | Model Number SM-40HF-B-d-c; 40KW 55C, Mobile X-ray system recalled | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | Starcam/Camstar recalled by Ge Medical Systems Israel | GE Medical Systems Israel Functional Imaging | Other | |
| Device | CLASS I | IV Administration sets recalled by ICU Medical | ICU Medical | Other | Nationwide |
| Device | CLASS II | Millenium Myosight recalled by Ge Medical Systems Israel | GE Medical Systems Israel Functional Imaging | Other | |
| Device | CLASS II | Model Number 40KWFXPLUS.889, Mobile X-ray system recalled by Sedecal | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | SM_40HF_B_D_VIR3.004, Mobile X-ray system recalled by Sedecal | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | Model Number SM-40HF-B-d-c; 40KW.005, Mobile X-ray system recalled | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | Model SM-40HF-B-d-c; 40KW - Canon Ready, Mobile X-ray system recalled | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | Model Number 40KWFXPLUS-710CW.007, Mobile X-ray system recalled | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | BD EpiCenter Microbiology Data Management System recalled | Becton Dickinson | Other | Nationwide |
| Device | CLASS II | iNSitu Bipolar Hip System, Bipolar head implant Part ID recalled | Theken Companies | Sterility | Nationwide |
| Device | CLASS II | Millenium MG/MC; dual-head nuclear medicine gamma camera recalled | GE Medical Systems Israel Functional Imaging | Other | |
| Device | CLASS II | Model Number 40KW-FX.899, Mobile X-ray system recalled by Sedecal | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | Model Number SM-40HF-B-d-c; 40KW.002, Mobile X-ray system recalled | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | Shanghai United Imaging Healthcare Co., Ltd recalled by UIH Technologies | UIH Technologies | Other | TX |
| Device | CLASS II | Elscint Model 4XX; dual-head nuclear medicine gamma camera designed recalled | GE Medical Systems Israel Functional Imaging | Other | |
| Device | CLASS II | Shanghai United Imaging Healthcare Co., Ltd recalled by UIH Technologies | UIH Technologies | Other | TX |
| Device | CLASS II | Shimadzu RF.004, Mobile X-ray system recalled by Sedecal | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | Shanghai United Imaging Healthcare Co., Ltd recalled by UIH Technologies | UIH Technologies | Other | TX |
| Device | CLASS II | GE Healthcare Carescape Central Station (CSCS) V3 MAS800 Desktop recalled | Wipro GE Healthcare Private | Device Malfunction | |
| Device | CLASS II | 1180264408 Salem Sump" PVC Gastroduodenal Tube/Ch recalled | Cardinal Health 200 | Device Malfunction | Nationwide |
| Device | CLASS II | Model Number SM-20HF-Batt; 20KW Analog, Mobile X-ray system recalled | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | SM_40HF_BDC3, Mobile X-ray system recalled by Sedecal | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | SM_40HF_B_D_VIR3, Mobile X-ray system recalled by Sedecal | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | Model Number SM-40HF-B-d-c; 40KW 70C, Mobile X-ray system recalled | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | Millenium MPR recalled by Ge Medical Systems Israel | GE Medical Systems Israel Functional Imaging | Other | |
| Device | CLASS II | Zenition 50; Product Number recalled by Philips Medical Systems | Philips Medical Systems Nederl | Other | MO, TX |
| Device | CLASS II | Model Number SM-40HF-B-d-c; 40KW, Mobile X-ray system recalled | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | t:slim X2 insulin pump with Interoperable Technology recalled | Tandem Diabetes Care | Device Malfunction | Nationwide |
| Device | CLASS II | Fuse Ultra Foot Plating System Instructions for Use recalled | CPM Medical Consultants | Sterility | Nationwide |
| Device | CLASS II | 264929 Salem Sump" Stomach Tube recalled by Cardinal Health 200 | Cardinal Health 200 | Device Malfunction | Nationwide |
| Device | CLASS II | Shanghai United Imaging Healthcare Co., Ltd recalled by UIH Technologies | UIH Technologies | Other | TX |
| Device | CLASS II | Shanghai United Imaging Healthcare Co., Ltd recalled by UIH Technologies | UIH Technologies | Other | TX |
| Device | CLASS II | Model Number SM-40HF-B-d-c; 40KW 55C/60C, Mobile X-ray system recalled | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | Model Number 40KWFXPLUS.004, Mobile X-ray system recalled by Sedecal | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | 8888265108 Salem Sump Silicone Dual Lumen Stomach Tube recalled | Cardinal Health 200 | Device Malfunction | Nationwide |
| Device | CLASS II | Model Number SM-32HF-B-d-c; 32KW 50G, Mobile X-ray system recalled | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | Oral Probe recalled by Baxter Healthcare | Baxter Healthcare | Temperature Abuse | Nationwide |
| Device | CLASS II | Elscint SPX6 recalled by Ge Medical Systems Israel | GE Medical Systems Israel Functional Imaging | Other | |
| Device | CLASS II | MobileDiagnost wDR recalled by Sedecal | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | Excelsior Medical, 0.9% Sodium Chloride Injection, USP - Fill recalled | Medline Industries | Device Malfunction | Nationwide |
| Drug | CLASS II | Opdualag (nivolumab and relatlimab-rmbw) injection recalledOpdualag | Bristol-Myers Squibb | Sterility | Nationwide |
| Drug | CLASS II | Ketorolac Tromethamine Injection, USP, 60 mg recalled by Aspiro PharmaKetorolac Tromethamine | Aspiro Pharma | Particulate Matter | Nationwide |
| Drug | CLASS II | Zicam" Medicated Fruit Drops Elderberry Flavor, 25-drops recalledZicam Cold Remedy Medicated Fruit Drops - Elderberry | Church & Dwight | Packaging Defects | Nationwide |
| Drug | CLASS III | Cetirizine Hydrochloride Tablets USP 10 mg recalled by JB Chemicals andCetirizine Hydrochloride | JB Chemicals and Pharmaceuticals | Other | Nationwide |
| Drug | CLASS II | Gabapentin Capsules, USP, 100 mg ( blister packs) recalled | The Harvard Drug Group | Potency & Assay | Nationwide |
| Drug | CLASS II | Medline, Alcohol Prep Pads (2-Ply Pad recalled by Medline Industries | Medline Industries | Potency & Assay | Nationwide |
| Drug | CLASS II | Olopatadine Hydrochloride Ophthalmic Solution USP 0.1 % recalled | USV Private | Potency & Assay | Nationwide |
| Drug | CLASS II | Taoscare Motion Sickness Patches recalled by ibspot | ibspot | Other | VA, WY |
| Drug | CLASS III | Cetirizine Hydrochloride Tablets USP 10 mg recalled by JB Chemicals andCetirizine Hydrochloride | JB Chemicals and Pharmaceuticals | Other | Nationwide |
| Drug | CLASS II | Gabapentin Capsules, USP, 100 mg ( blister pack) recalledGabapentin | The Harvard Drug Group | Potency & Assay | Nationwide |
| Drug | CLASS II | Niacin Extended-release Tablets, USP, 1,000 mg recalledNiacin | Lannett | Potency & Assay | Nationwide |
| Drug | CLASS II | Bupropion Hydrochloride Extended-Release Tablets USP (XL), 300 mg recalledBupropion Hydrochloride | Graviti Pharmaceuticals Private | Other | Nationwide |
| Food | CLASS I | Scott & Jon s Shrimp Scampi with Linguine recalled by Demers Food GroupScott | Demers Food Group | Listeria | Nationwide |
| Food | CLASS II | Oceans Kitchen Imitation Crabmeat Shredded Made From Wild recalledOceans | Ocean's Kitchen | Botulism | WA |
| Food | CLASS II | Arctic Shores recalled by Southwind FoodsArctic Shores | Southwind Foods | Other | 34 states |
| Food | CLASS I | Cheese and Egg with Green Salsa Breakfast Burrito;;/case recalled | M.C.I. Foods | Listeria | Nationwide |
| Food | CLASS I | Wegmans Brulee Cheesecake Large recalled by Wegmans Food MarketsWegmans Brulee | Wegmans Food Markets | Undeclared Tree Nuts | MD, NC, VA |
| Food | CLASS I | Thick Shanghai Style Plain Noodle recalled by Twin MarquisTwin Marquis | Twin Marquis | Undeclared Egg | 6 states |
| Food | CLASS I | Smoked Mozzarella Penne Salad-Small, Clam shell and Bowl recalled | Giant Eagle | Listeria | 4 states |
| Food | CLASS I | Large Ultimate Fresh Fruit Topped Cheesecake recalled | Wegmans Food Markets | Undeclared Tree Nuts | MD, NC, VA |
| Food | CLASS II | Organic Iqf Chopped Spinach recalled by Del Mar Food Products | Del Mar Food Products | Listeria | MN |
| Food | CLASS I | Basil Pesto Bowtie Pasta Salad recalled by Albertsons CompaniesBasil Pesto | Albertsons Companies | Listeria | 15 states |
| Food | CLASS I | Floria Dried Apricots packages, 40 packages recalled by Turkana FoodFloria | Turkana Food | Undeclared Sulfites | 18 states |
| Food | CLASS II | Rolling Pin Dubai Style Chocolate recalledRolling Pin | Rolling Pin Baking Company | Undeclared Wheat & Gluten | 14 states |
| Food | CLASS I | Ready Meals Basil Pesto Bowtie Pasta Salad recalled | Albertsons Companies | Listeria | 15 states |
| Food | CLASS II | Ben's Original Ready Rice Original Long Grain White recalledBen's | Mars Foods Us | Other | 9 states |
| Food | CLASS II | Lunds & Byerly's Premium confections recalled by Abdallah IncorporatedLunds | Abdallah Incorporated | Undeclared Tree Nuts | MN |
| Food | CLASS II | Great American branded Frozen raw shrimp skewer recalledGreat | Southwind Foods | Other | 34 states |
| Food | CLASS II | Lmps 1.5" Bulk Mozzarella recalled by Leprino FoodsLmps | Leprino Foods | Foreign Material | 5 states |
| Food | CLASS I | Wegmans Large Ultimate Strawberry Topped Cheesecake recalledWegmans | Wegmans Food Markets | Undeclared Tree Nuts | MD, NC, VA |
| Food | CLASS I | Smoked Mozzarella Penne Salad Kit recalled by Albertsons Companies | Albertsons Companies | Listeria | 15 states |
| Food | CLASS II | Sprite Can 49000058482 / JUN2926MAA Sprite Can recalledSprite Can | Cocacola Southwest Beverages | Foreign Material | TX |
| Food | CLASS I | Smoked Mozzarella Penne Salad recalled by The Kroger | The Kroger | Listeria | 28 states |
| Food | CLASS I | Basil Pesto Bowtie Pasta Salad recalled by The KrogerBasil Pesto | The Kroger | Listeria | 28 states |
| Food | CLASS II | Arctic Shores branded Frozen cooked salad shrimp recalledArctic Shores | Southwind Foods | Other | 34 states |
| Food | CLASS I | Wegmans Large Ultimate Cherry Topped Cheesecake recalledWegmans | Wegmans Food Markets | Undeclared Tree Nuts | MD, NC, VA |
| Food | CLASS II | Arctic Shores recalled by Southwind FoodsArctic Shores | Southwind Foods | Other | 34 states |
| Food | CLASS I | Fresh Creative Foods (FCF) recalled by Reser's Fine Foods | Reser's Fine Foods | Listeria | 13 states |
| Food | CLASS I | Ready Meals Spinach Bowtie Pasta Salad recalled by Albertsons Companies | Albertsons Companies | Listeria | 15 states |
| Food | CLASS I | Fresh Creative Foods (FCF) recalled by Reser's Fine Foods | Reser's Fine Foods | Listeria | 13 states |
| Food | CLASS I | Sprouts Smoked Mozzarella Pasta Salad, RTE Pasta Salad recalledSprouts | Sprouts Farmers Market | Listeria | 24 states |
| Food | CLASS I | Ready Meals Smoked Mozzarella Penne Pasta Salad recalled | Albertsons Companies | Listeria | 15 states |
| Food | CLASS I | Basil Pesto Bowtie Pasta Salad recalled by Albertsons CompaniesBasil Pesto | Albertsons Companies | Listeria | 15 states |
| Food | CLASS I | Smoked Mozzarella Penne Salad-Large, Clam shell and Bowl recalled | Giant Eagle | Listeria | 4 states |
| Food | CLASS II | Ben's Original Ready Rice Whole Grain Brown recalled by Mars Foods UsBen's | Mars Foods Us | Other | 9 states |
| Food | CLASS II | Coca-Cola Zero Sugar Can - 49000042559 / FEB0226MAA recalledCoca-Cola Zero | Cocacola Southwest Beverages | Foreign Material | TX |
| Food | CLASS II | tru fru Strawberries + Creme Freeze-Dried Fresh, retail recalled | Georgia Nut | Foreign Material | IL |
| Food | CLASS I | Smoked Mozzarella Penne Salad, bulk recalled by Giant Eagle | Giant Eagle | Listeria | 4 states |
| Food | CLASS I | Grilled Chicken & Basil Pasta Extra Large recalledGrilled | Albertsons Companies | Listeria | 15 states |
| Food | CLASS II | tru fru Dark + White Chocolate Freeze-Dried Strawberries recalled | Georgia Nut | Foreign Material | IL |
| Food | CLASS I | Wegmans Large Ultimate Plain Cheesecake recalled by Wegmans Food MarketsWegmans | Wegmans Food Markets | Undeclared Tree Nuts | MD, NC, VA |
| Food | CLASS II | Ben's Original Ready Rice Long Grain & Wild recalled by Mars Foods UsBen's | Mars Foods Us | Other | 9 states |
| Food | CLASS II | Coca-Cola Can - 49000012781 / JUN2926MAA Coca-Cola Can recalledCoca-Cola Can | Cocacola Southwest Beverages | Foreign Material | TX |
| Food | CLASS I | Egg and Cheese Breakfast Burrito;;/case recalled by M.C.I. Foods | M.C.I. Foods | Listeria | Nationwide |
| Food | CLASS II | Jumbo Meat Ball Sub recalled by Mg Foods | Mg Foods | Foreign Material | LA, TX |
| Food | CLASS I | Ready Meals Basil Bowtie Pasta Salad recalled by Albertsons Companies | Albertsons Companies | Listeria | 15 states |
| Food | CLASS I | Ready Meals Pesto Bowtie Pasta Salad recalled by Albertsons Companies | Albertsons Companies | Listeria | 15 states |
| Food | CLASS I | Wegmans Large Ultimate Blueberry Topped Cheesecake recalledWegmans | Wegmans Food Markets | Undeclared Tree Nuts | MD, NC, VA |
| Food | CLASS II | Tovala branded Frozen raw phosphate free shrimp recalledTovala | Southwind Foods | Other | 34 states |
| Food | CLASS II | Frozen Organic Spinach recalled by Sno Pac Foods | Sno Pac Foods | Listeria | 12 states |
| Food | CLASS I | Ready Meals Smoked Mozzarella With Hot Links Extra Large recalled | Albertsons Companies | Listeria | 15 states |
| Food | CLASS I | Fresh Creative Foods (FCF) recalled by Reser's Fine Foods | Reser's Fine Foods | Listeria | 13 states |
| Food | CLASS I | Pulled Pork Sandwich Products recalled by E.A. Sween | E.A. Sween | Foreign Material | |
| Food | CLASS I | Ready-To-Eat Frozen Chicken Products recalled by Hormel Foods | Hormel Foods | Foreign Material | |
| Food | CLASS I | BBQ Pork Jerky Product recalled by Link Snacks | Link Snacks | Foreign Material | |
| Device | CLASS II | Clearlink System Solution Set, Non-Vented recalled by Baxter Healthcare | Baxter Healthcare | Packaging Defects | Nationwide |
| Device | CLASS II | Flow Re-Direction Endoluminal Devices: FRED recalled by Microvention | Microvention | Other | Nationwide |
| Device | CLASS I | Bronchovideoscope Olympus Bf-q170 recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Clearlink System Extension Set, Straight-Type Extension Set recalled | Baxter Healthcare | Packaging Defects | Nationwide |
| Device | CLASS I | TactiFlex Sensor Enabled Ablation Catheter, 8F, DF, (BiD Curve D-F) recalled | Abbott | Packaging Defects | MN |
| Device | CLASS I | Model Number S722, Altrua 2 DR EL Pacemaker recalled | Boston Scientific | Device Malfunction | MN |
| Device | CLASS II | Medical convenience kits recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS I | Oes Bronchofiberscope Olympus Bf Type Mp60 recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS I | Proponent Dr Sl recalled by Boston Scientific | Boston Scientific | Device Malfunction | MN |
| Device | CLASS II | Medical convenience kits recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | Femoral Head (Ceramic heads 28-30) Product ID/Description recalled | BioPro | Sterility | MI, TX |
| Device | CLASS II | CX Preconnect with Tenacio Pump with InhibiZone recalled | Boston Scientific | Other | Nationwide |
| Device | CLASS I | Evis Exera Ii Bronchovideoscope Olympus Bf Type Q180 recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Medical convenience kits recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS I | Evis Exera Ii Bronchovideoscope Olympus Bf Type 1tq180 recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Medical convenience kits recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS I | Model Number L100, Essentio SR SL Pacemaker recalled | Boston Scientific | Device Malfunction | MN |
| Device | CLASS II | Endo Head (Metal uni-polar, 38-55) Product recalled by BioPro | BioPro | Sterility | MI, TX |
| Device | CLASS II | Neuroguard IEP 1 Carotid Stent recalled by Contego Medical | Contego Medical | Device Malfunction | Nationwide |
| Device | CLASS II | Cardiac Workstation recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Adult Anesthesia Set recalled by Medline Industries | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Clearlink System Continu-flo Solution Set, Non-Vented recalled | Baxter Healthcare | Packaging Defects | Nationwide |
| Device | CLASS II | LGX Preconnect with Tenacio Pump with InhibiZone recalled | Boston Scientific | Other | Nationwide |
| Device | CLASS II | DuoDERM" Extra Thin dressings are highly flexible recalled by ConvaTec | ConvaTec | Foreign Material | Nationwide |
| Device | CLASS I | Evis Exera Iii Bronchovideoscope Olympus Bf-1th190 recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS I | Oes Bronchofiberscope Olympus Bf Type P60 recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Medical convenience kits recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | Logiq P10 series recalled by GE Medical Systems | GE Medical Systems | Labeling Errors | Nationwide |
| Device | CLASS I | Model Number S701 Altrua 2 SR SL Pacemaker recalled by Boston Scientific | Boston Scientific | Device Malfunction | MN |
| Device | CLASS II | CX Preconnect with Tenacio Pump without InhibiZone recalled | Boston Scientific | Other | Nationwide |
| Device | CLASS II | CXR Preconnect with Tenacio Pump with InhibiZone recalled | Boston Scientific | Other | Nationwide |
| Device | CLASS II | Medical convenience kits recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS I | TactiFlex Sensor Enabled Ablation Catheter, 8F, F, (UniD Curve F) recalled | Abbott | Packaging Defects | MN |
| Device | CLASS I | Evis Exera Iii Bronchovideoscope Olympus Bf-p190 recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS I | Accolade Dr El recalled by Boston Scientific | Boston Scientific | Device Malfunction | MN |
| Device | CLASS II | Xerf Effector Electrosurgical unit recalled by Lutronic | Lutronic | Device Malfunction | Nationwide |
| Device | CLASS II | Femoral Head Product ID/Description 14089 Head Femoral recalled | BioPro | Sterility | MI, TX |
| Device | CLASS II | Medical convenience kits recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | Medical convenience kits recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | Endo Head (Ceramic) Product ID/Description 13006 Endo recalled by BioPro | BioPro | Sterility | MI, TX |
| Device | CLASS II | Branding is not applied to this product DVI display cables recalled | Spacelabs Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Medical convenience kits recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | Medical convenience kits UDPG88W PICC G-tube Pack recalled | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | Clearlink System Continu-flo Solution Set, Non-Vented recalled | Baxter Healthcare | Packaging Defects | Nationwide |
| Device | CLASS I | Evis Exera b Bronchovideoscope Olympus Bf-XT190 recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | The failure occurs if a user on the Omnipod 5 iOS recalled by Insulet | Insulet | Device Malfunction | Nationwide |
| Device | CLASS I | Evis Exera Iii Bronchovideoscope Olympus Bf-q190 recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Clearlink System Continu-flo Solution Set, Non-Vented recalled | Baxter Healthcare | Packaging Defects | Nationwide |
| Device | CLASS II | Basic Biopsy Tray recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | Logiq P9 R4.5 ultrasound system with system recalled | GE Medical Systems | Labeling Errors | Nationwide |
| Device | CLASS II | The CycloPen Microinterventional Cyclodialysis device recalled | Iantrek | Sterility | Nationwide |
| Device | CLASS I | Bronchovideoscope Olympus Bf Type 1t150 recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Airvo 2, REF: PT101US, and myAirvo 2, REF: PT100US, used recalled | Fisher & Paykel Healthcare | Other | Nationwide |
| Device | CLASS I | Zenith Alpha 2 Thoracic Endovascular Graft recalled | Cook Medical | Other | 27 states |
| Device | CLASS I | Bronchovideoscope Olympus Bf-h1100 recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Medical convenience kits recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | The C-Rex UNO Microinterventional Goniotomy Instrument recalled | Iantrek | Sterility | Nationwide |
| Device | CLASS II | Branding is not applied to this product DVI display cables recalled | Spacelabs Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Clearlink System Non_DEHP Extenstion Set recalled by Baxter Healthcare | Baxter Healthcare | Packaging Defects | Nationwide |
| Device | CLASS II | Basic Biopsy Tray recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | Clearlink System Extension Set, Straight-Type Extension Set recalled | Baxter Healthcare | Packaging Defects | Nationwide |
| Device | CLASS II | Continu-flo Solution Set, Non-Vented recalled by Baxter Healthcare | Baxter Healthcare | Packaging Defects | Nationwide |
| Device | CLASS II | Clearlink System Paclitaxel Set, Non-Vented recalled | Baxter Healthcare | Packaging Defects | Nationwide |
| Device | CLASS II | Medical convenience kits IHDC30R D AND C PACK recalled | American Contract Systems | Sterility | Nationwide |
| Device | CLASS I | Model Number L221 Proponent DR EL Pacemaker recalled | Boston Scientific | Device Malfunction | MN |
| Device | CLASS II | Arvis" Shoulder recalled by Kico Knee Innovation | Kico Knee Innovation | Device Malfunction | Nationwide |
| Device | CLASS II | Clearlink System Non-dehp Continu-flo Soln Set, 96" (2,4 m) recalled | Baxter Healthcare | Packaging Defects | Nationwide |
| Device | CLASS II | LGX Preconnect with Tenacio Pump without InhibiZone recalled | Boston Scientific | Other | Nationwide |
| Device | CLASS I | Proponent SR Sl recalled by Boston Scientific | Boston Scientific | Device Malfunction | MN |
| Device | CLASS I | Evis Exera Ii Bronchovideoscope Olympus Bf Type P180 recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Clearlink System Continu-flo Solution Set, Non-Vented recalled | Baxter Healthcare | Packaging Defects | Nationwide |
| Device | CLASS II | Branding is not applied to this product DVI display cables recalled | Spacelabs Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Tenacio Pump with InhibiZone recalled by Boston Scientific | Boston Scientific | Other | Nationwide |
| Device | CLASS II | STA Liatest D-Di recalled by Diagnostica Stago | Diagnostica Stago | Other | Nationwide |
| Device | CLASS I | Evis Exera Iii Bronchovideoscope Olympus Bf-h190 recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS I | Phasitron 5, IPV In-Line Valve recalled by Percussionaire | Percussionaire | Packaging Defects | Nationwide |
| Device | CLASS I | Bronchofiberscope Olympus Bf Type Pe2 recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS I | Model Number U226, Visionist Crt-p EL recalled by Boston Scientific | Boston Scientific | Device Malfunction | MN |
| Device | CLASS II | Medical convenience kits recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS I | Bronchovideoscope Olympus Bf-1tq170 recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS I | Model Number L209 Proponent DR (VDD) SL Pacemaker recalled | Boston Scientific | Device Malfunction | MN |
| Device | CLASS I | TactiFlex Sensor Enabled Ablation Catheter, 8F, D, (UniD Curve D) recalled | Abbott | Packaging Defects | MN |
| Device | CLASS I | Evis Exera Ii Bronchovideoscope Olympus Bf Type Q180-ac recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Clearlink System Continu-flo Solution Set, Non-Vented recalled | Baxter Healthcare | Packaging Defects | Nationwide |
| Device | CLASS II | Femoral Head (Metal 22, 28, 32, 36, cobalt chromium recalled by BioPro | BioPro | Sterility | MI, TX |
| Device | CLASS II | Cardiac Workstation recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS I | Bronchovideoscope Olympus Bf-1th1100 recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Clearlink System Extension Set, Straight-Type Extension Set recalled | Baxter Healthcare | Packaging Defects | Nationwide |
| Device | CLASS II | Medical convenience kits recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | Medical convenience kits recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS I | Evis Exera Ii Bronchovideoscope Olympus Bf Type 1t180 recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Echelon Linear Cutters Reload Blue, intended recalled | Ethicon Endo-Surgery | Other | OH |
| Device | CLASS II | Bipolar Head Product ID/Description 18130 Bipolar Head recalled | BioPro | Sterility | MI, TX |
| Device | CLASS I | Bronchovideoscope Olympus Bf Type P150 recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Tenacio Pump without InhibiZone recalled by Boston Scientific | Boston Scientific | Other | Nationwide |
| Device | CLASS II | Ferno Power X2 Powered Ambulance Cot recalled by Ferno-Washington | Ferno-Washington | Other | Nationwide |
| Device | CLASS II | Clearlink System Continu-flo Solution Set, Non-Vented recalled | Baxter Healthcare | Packaging Defects | Nationwide |
| Device | CLASS I | TactiFlex Sensor Enabled Ablation Catheter, 8F, DD, (BiD Curve D-D) recalled | Abbott | Packaging Defects | MN |
| Device | CLASS I | Oes Bronchofiberscope Olympus Bf Type 1t60 recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS I | Bronchofiberscope Olympus Bf Type Te2 recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS I | TactiFlex Sensor Enabled Ablation Catheter, 8F, FJ, (BiD Curve F-J) recalled | Abbott | Packaging Defects | MN |
| Device | CLASS I | Oes Bronchofiberscope Olympus Bf Type Xt40 recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Logiq P10 R4.5 HD ultrasound system with system recalled | GE Medical Systems | Labeling Errors | Nationwide |
| Device | CLASS II | Medical convenience kits recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | Clearlink System Continu-flo Solution Set, Non-Vented recalled | Baxter Healthcare | Packaging Defects | Nationwide |
| Device | CLASS I | Model Number S702, Altrua 2 DR SL Pacemaker recalled | Boston Scientific | Device Malfunction | MN |
| Device | CLASS I | Evis Exera Bronchovideoscope Olympus Bf Type Xt160 recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Clearlink System Solution Set, Duo-vent recalled by Baxter Healthcare | Baxter Healthcare | Packaging Defects | Nationwide |
| Drug | CLASS II | Aloe Up Sport Performance Sunscreen Lotion SPF 30 per tube recalled | SV Labs Prescott | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS III | Everolimus tablets 5mg (each carton contains 4 blister recalled | Endo USA | Potency & Assay | Nationwide |
| Drug | CLASS II | Viorele, Desogestrel and Ethinyl Estradiol recalledViorele | Glenmark Pharmaceuticals Inc., USA | Potency & Assay | Nationwide |
| Drug | CLASS III | FentaNYL Citrate PF, 500mcg/ (10mcg/mL) in Nacl recalled by STAQ Pharma | Staq Pharma | Other | Nationwide |
| Drug | CLASS III | Hydromorphone HCL PF, 10mg/ (0.2mg/mL) in Nacl recalled by STAQ Pharma | Staq Pharma | Other | Nationwide |
| Drug | CLASS II | Atorvastatin Calcium Tablets USP, 40 mg recalled by Ascend LaboratoriesAtorvastatin Calcium | Ascend Laboratories | Potency & Assay | Nationwide |
| Drug | CLASS II | Atorvastatin Calcium Tablets USP, 10 mg recalled by Ascend LaboratoriesAtorvastatin Calcium | Ascend Laboratories | Potency & Assay | Nationwide |
| Drug | CLASS I | Oxytocin in 0.9% Sodium Chloride for intravenous use recalled | IntegraDose Compounding Services | Potency & Assay | Nationwide |
| Drug | CLASS II | Fasenra (benralizumab) Injection, 30 mg/mL recalledFasenra | Astrazeneca Pharmaceuticals | Sterility | Nationwide |
| Drug | CLASS II | Sucralfate Tablets recalled by Amerisource Health Services | Amerisource Health Services | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Atorvastatin Calcium Tablets USP, 20 mg recalled by Ascend LaboratoriesAtorvastatin Calcium | Ascend Laboratories | Potency & Assay | Nationwide |
| Drug | CLASS III | Ketamine Hydrochloride, 50mg/ (10mg/mL), Injection recalled | Staq Pharma | Other | Nationwide |
| Drug | CLASS II | Tavaborole Topical solution recalled by Viona PharmaceuticalsTavaborole | Viona Pharmaceuticals | Other | Nationwide |
| Drug | CLASS II | Carbidopa, Levodopa, Entacapone Tablets, 25 mg/100 mg/200 mg recalledCarbidopa, Levodopa And Entacapone | Rising Pharma Holding | Packaging Defects | Nationwide |
| Drug | CLASS II | Atorvastatin Calcium Tablets USP, 80 mg recalled by Ascend LaboratoriesAtorvastatin Calcium | Ascend Laboratories | Potency & Assay | Nationwide |
| Food | CLASS II | Gluten Free Bean & Rice Burrito recalled by Amy's Kitchen | Amy's Kitchen | Foreign Material | 21 states |
| Food | CLASS II | NOW Real Food Organic Unsalted Whole Raw Cashews recalledNOW Real | Now Foods | Undeclared Allergens | Nationwide |
| Food | CLASS I | Free Range Grade AA Large Brown Eggs, Loose Pack recalled | Black Sheep Egg Company | Salmonella | 6 states |
| Food | CLASS I | Wegmans Ultimate Plain Cheesecake Large recalled by Eli's CheesecakeWegmans Ultimate | Eli's Cheesecake | Undeclared Tree Nuts | PA, VA |
| Food | CLASS I | Bona Fish recalled by Vicky ITBona | Vicky IT | Mold | NY |
| Food | CLASS I | Cut Fresh Fruit Mix recalled by Wholesale Produce SupplyCut | Wholesale Produce Supply | Listeria | 5 states |
| Food | CLASS I | Free Range Grade AA Medium Brown Eggs, Loose Open Skid recalled | Black Sheep Egg Company | Salmonella | 6 states |
| Food | CLASS II | Good and Gather Southwest-Style Burrito Bowl Blend recalledGather | One Frozen | Undeclared Fish & Shellfish | Nationwide |
| Food | CLASS I | Haifa Cold Smoked Seabass recalled by D & M Smoked FishHaifa Cold | D & M Smoked Fish | Listeria | 7 states |
| Food | CLASS I | Cut Fresh Fruit Tray with Strawberries recalledCut | Wholesale Produce Supply | Listeria | 5 states |
| Food | CLASS II | Wise Wife Ground Cinnamon recalled by SLR Food DistributionWise Wife | SLR Food Distribution | Lead & Heavy Metals | 5 states |
| Food | CLASS I | Harvest Cuts Fruit Tray with Watermelons recalledHarvest Cuts | Wholesale Produce Supply | Listeria | 5 states |
| Food | CLASS II | Pears Sliced in Organic Pear Juice from Concentrate recalledPears | Pacific Coast Producers | Foreign Material | 27 states |
| Food | CLASS I | Free Range Grade AA Medium White Eggs, 15dz recalled | Black Sheep Egg Company | Salmonella | 6 states |
| Food | CLASS II | Pears Halves in Pear Juice from Concentrate recalledPears Halves | Pacific Coast Producers | Foreign Material | 27 states |
| Food | CLASS I | Cut Fresh Melon Mix recalled by Wholesale Produce SupplyCut | Wholesale Produce Supply | Listeria | 5 states |
| Food | CLASS I | Cut Fresh Cantaloupe & Honeydew Chunks Fresh & Finest recalledCut | Wholesale Produce Supply | Listeria | 5 states |
| Food | CLASS I | Free Range Grade A Large Brown Eggs recalled by Black Sheep Egg Company | Black Sheep Egg Company | Salmonella | 6 states |
| Food | CLASS I | Free Range Grade AA Large White Eggs, Loose Open Skid recalled | Black Sheep Egg Company | Salmonella | 6 states |
| Food | CLASS I | Cut Fresh Luau Blend Fruit Mix "F&F". Fresh & Finest recalledCut | Wholesale Produce Supply | Listeria | 5 states |
| Food | CLASS I | Cut Fresh Fruit Salad recalled by Wholesale Produce SupplyCut | Wholesale Produce Supply | Listeria | 5 states |
| Food | CLASS I | Cut Fresh Fruit Mix recalled by Wholesale Produce SupplyCut | Wholesale Produce Supply | Listeria | 5 states |
| Food | CLASS I | Free Range Grade AA Large White Eggs, 15dz recalled | Black Sheep Egg Company | Salmonella | 6 states |
| Food | CLASS II | Sea Port Raw Frozen Easy Peel Headless Shell-On White recalledSea Port | Sea Port Products | Other | 5 states |
| Food | CLASS II | Fruit Cocktail IN 100% Juice With Added Ingredients recalled | Pacific Coast Producers | Foreign Material | 27 states |
| Food | CLASS II | Wawa Strawberry Lemonade (Pint), Stored refrigerated recalledWawa | Wawa Beverage | Foreign Material | 4 states |
| Food | CLASS I | Sliced (1/4") green onions, refrigerated recalled by Garden Fresh Foods | Garden Fresh Foods | Listeria | WA |
| Food | CLASS I | Cut Fresh Fruit with Fruit Dip recalled by Wholesale Produce SupplyCut | Wholesale Produce Supply | Listeria | 5 states |
| Food | CLASS I | Free Range Grade AA Large Brown Eggs, Loose Open Skid recalled | Black Sheep Egg Company | Salmonella | 6 states |
| Food | CLASS II | Wawa HVD (Whole) Milk (Pint), Stored refrigerated recalledWawa HVD | Wawa Beverage | Foreign Material | 4 states |
| Food | CLASS II | Wawa Strawberry Milk, Lowfat Milk (Pint), Stored refrigerated recalledWawa | Wawa Beverage | Foreign Material | 4 states |
| Food | CLASS I | Cut Fresh Cantaloupe Chunks packaged into the following recalledCut | Wholesale Produce Supply | Listeria | 5 states |
| Food | CLASS II | Silver Horse - Pure Aluminium recalled by Goyal Group | Goyal Group | Lead & Heavy Metals | 13 states |
| Food | CLASS II | Halved Pears IN Pear Juice From Concnetrate recalledHalved Pears | Pacific Coast Producers | Foreign Material | 27 states |
| Food | CLASS I | Haifa Cold Smoked Salmon recalled by D & M Smoked FishHaifa Cold | D & M Smoked Fish | Listeria | 7 states |
| Food | CLASS I | Free Range Grade AA Medium White Eggs, Loose Open Skid recalled | Black Sheep Egg Company | Salmonella | 6 states |
| Food | CLASS II | 6+ Months Sprout Organics Made With Organic Sweet Potato recalled | Sprout Organics | Foreign Material | 34 states |
| Food | CLASS II | Dole Apple Juice (primary package), PET, Refrigerate after opening recalledDole | Tropicana Brands Group | Mold | 11 states |
| Food | CLASS I | Free Range Grade AA Medium Brown Eggs, Loose Pack recalled | Black Sheep Egg Company | Salmonella | 6 states |
| Food | CLASS I | Free Range Grade A Large Brown Eggs recalled by Black Sheep Egg Company | Black Sheep Egg Company | Salmonella | 6 states |
| Food | CLASS I | Cut Fresh Fruit Mix recalled by Wholesale Produce SupplyCut | Wholesale Produce Supply | Listeria | 5 states |
| Food | CLASS I | Ready-To-Eat Breakfast Burrito and Wrap Products recalled | M.C.I. Foods | Listeria | |
| Device | CLASS II | Ce17tfc Continuous Epid Set W/ Tuohy recalled by B Braun Medical | B Braun Medical | Other | Nationwide |
| Device | CLASS I | NOxBOXi Nitric Oxide Delivery System recalled | Noxbox | Other | TN |
| Device | CLASS II | Artegraft Collagen Vascular Graft recalled by LeMaitre Vascular | LeMaitre Vascular | Labeling Errors | NJ |
| Device | CLASS II | NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 recalled | Applied Medical Technology | Other | MA, RI |
| Device | CLASS II | NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 recalled | Applied Medical Technology | Other | MA, RI |
| Device | CLASS II | FDR Visionary Suite recalled by FUJIFILM Healthcare Americas | Fujifilm Healthcare Americas | Device Malfunction | 8 states |
| Device | CLASS II | Ce17tkf Perifix Contin recalled by B Braun Medical | B Braun Medical | Other | Nationwide |
| Device | CLASS II | Optiflux¿ High Flux E-beam Dialyzer recalled by Fresenius Medical Care | Fresenius Medical Care Holdings | Other | Nationwide |
| Device | CLASS II | Ce17tkfsdt Epid Tray W/ Fixed Wing recalled by B Braun Medical | B Braun Medical | Other | Nationwide |
| Device | CLASS II | Ce17tkfcs Cont Epid Tray W/ Tuohy-lf recalled by B Braun Medical | B Braun Medical | Other | Nationwide |
| Device | CLASS II | Synchron Systems Phosphorus (PHOSm) Reagent recalled by Beckman Coulter | Beckman Coulter | Other | 14 states |
| Device | CLASS II | NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 recalled | Applied Medical Technology | Other | MA, RI |
| Device | CLASS II | FlexLab (FLX) System recalled by Inpeco | Inpeco | Other | CA, NY |
| Device | CLASS II | Design Options, Pain Management Tray recalled by B Braun Medical | B Braun Medical | Other | Nationwide |
| Device | CLASS II | Ce17tkfs Epidural Tray recalled by B Braun Medical | B Braun Medical | Other | Nationwide |
| Device | CLASS II | Design Options, Perifix FX Epidural Anesthesia Tray recalled | B Braun Medical | Foreign Material | Nationwide |
| Device | CLASS II | Ce17tbfc Epidural Basic Tray Touhy recalled by B Braun Medical | B Braun Medical | Other | Nationwide |
| Device | CLASS II | FlexLab X (FXX) System recalled by Inpeco | Inpeco | Other | CA, NY |
| Device | CLASS II | EverPatch+, REF: 1044002, Permanent Scleral Reinforcement Matrix recalled | Corneat Vision | Other | Nationwide |
| Device | CLASS II | Es1725kfx Espocan Spinal/epid recalled by B Braun Medical | B Braun Medical | Other | Nationwide |
| Device | CLASS II | ClariTEE Miniaturized TEE probe recalled by ImaCor | ImaCor | Other | Nationwide |
| Device | CLASS II | NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 recalled | Applied Medical Technology | Other | MA, RI |
| Device | CLASS II | CorNeat EverPatch recalled by Corneat Vision | Corneat Vision | Other | Nationwide |
| Device | CLASS II | Ce17tkfcps Epidural Full Tray recalled by B Braun Medical | B Braun Medical | Other | Nationwide |
| Device | CLASS I | Automated Impella Controller (AIC), used recalled by Abiomed | Abiomed | Packaging Defects | Nationwide |
| Device | CLASS II | Nes1727kfx W / Tuohy Sprw Ot recalled by B Braun Medical | B Braun Medical | Other | Nationwide |
| Device | CLASS II | Sesk Combined Spinal And Epidural Tray recalled by B Braun Medical | B Braun Medical | Other | Nationwide |
| Device | CLASS II | Ce17tkfc Epidural Tray W/ Tuohy recalled by B Braun Medical | B Braun Medical | Other | Nationwide |
| Device | CLASS II | This device is a digital radiography/fluoroscopy system recalled | Canon Medical System USA | Device Malfunction | CA |
| Device | CLASS I | BD Alaris Pump Infusion Sets recalled by CareFusion 303 | CareFusion 303 | Device Malfunction | Nationwide |
| Device | CLASS I | NOxBOXi Nitric Oxide Delivery System recalled | Noxbox | Device Malfunction | TN |
| Drug | CLASS II | Ultra Burn for Injection, all strengths and presentations recalled | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Semaglutide with B12 for Injection, all strengths recalled by GenoGenix | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Sterile Saline Reconstitution Solution for Injection recalled | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | B6 (Pyridoxine HCl) for Injections, all strengths recalled by GenoGenix | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Sermorelin Lyophilized powder for reconstitution, 10mg recalled | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | BPC-157/Thymosin Beta-4 for Injection, a) 10/10mg recalled by GenoGenix | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Low Solubility Peptide Reconstitution Solution recalled by GenoGenix | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | L-Arginine HCl for Injection, all strengths recalled by GenoGenix | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Succinylcholine Chloride Injection, USP, 200 mg/ (20 mg/mL) recalledSuccinylcholine | Dr. Reddy's Laboratories | Potency & Assay | Nationwide |
| Drug | CLASS II | Levothyroxine Sodium Tablets, USP, 88 mcg (0.088 mg) recalledLevothyroxine Sodium | Accord Healthcare | Potency & Assay | Nationwide |
| Drug | CLASS II | Thymosin Beta-4 (TB4) for Injection, 15mg recalled by GenoGenix | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Ascorbic Acid (Vitamin C) for Injection, Preserved recalled by GenoGenix | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Zinc Chloride for Injection, all strengths recalled by GenoGenix | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Bevacizumab 1.75 mg/ - syringe, Intravitreal Total Volume recalled | RC Outsourcing | Sterility | Nationwide |
| Drug | CLASS II | L-Glutamine for Injection, all strengths and presentations recalled | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Lipo MIC +B12 Methylcobalamin for Injection recalled by GenoGenix | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | CoQ10 for Injection, all strengths and presentations recalled | GenoGenix | Sterility | Nationwide |
| Drug | CLASS I | NAD+ (Nicotinamide adenine dinucleotide) for Injection recalled | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Zinc Sulfate for Injection, all strengths and presentations recalled | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Epithalon for Injection, 20mg, all presentations, GenoGenix recalled | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Pentosan for Injection, all strengths and presentations recalled | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | B-Complex for Injection, all strengths and presentations recalled | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Wyandotte, Sanifect E3, Hand Sanitizer (Ethanol-Based recalled | Acuity Specialty Products | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | GAC for Injection, all strengths and presentations recalled by GenoGenix | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Major ChlorproMAZINE Hydrochloride Tablets recalled | The Harvard Drug Group | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | B12 Methylcobalamin for Injection, all strengths recalled by GenoGenix | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Ascorbic Acid (Vitamin C) for Injection, Preservative Free recalled | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Elite Stack Reconstitution Solution for Injection recalled by GenoGenix | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Elite Stack MSC Exosome Reconstitution Solution recalled by GenoGenix | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | pH Buffered Reconstitution Solution for Injection recalled by GenoGenix | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Semaglutide for Injection, a) 20 mg b) 20 mg/mL Multi-Dose recalled | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Proline for Injection, all strengths and presentations recalled | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | B5 Dexpanthenol for Injection, all strengths recalled by GenoGenix | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Alpha Lipoic Acid for Injection, all strengths recalled by GenoGenix | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Lipo MIC + L-Carnitine for Injection, all strengths recalled | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Major ChlorproMAZINE Hydrochloride Tablets recalled | The Harvard Drug Group | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | EDTA for Injection, all strengths and presentations recalled | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | B12 Hydroxocobalamin for Injection, all strengths recalled by GenoGenix | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | AFCO, Hand Sanitizer (Isopropyl Alcohol-Based, Product 5515) recalled | Acuity Specialty Products | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Oxytocin for Injection, all strengths and presentations recalled | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Glutathione Preserved for Injection, all strengths recalled by GenoGenix | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Glutathione Magnesium for Injection, all strengths recalled by GenoGenix | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Doxycycline Hyclate Tablets, USP 100 mg* recalledDoxycycline | Acella Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Major ChlorproMAZINE Hydrochloride Tablets recalled | The Harvard Drug Group | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Major ChlorproMAZINE Hydrochloride Tablets, USP, 50 mg recalled | The Harvard Drug Group | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Retatrutide for Injection, 60mg / vial, all presentations recalled | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | BPC-157 for Injection, 15mg/ vial, all presentations recalled | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Vitamin D3 for Injection, all strengths and presentations recalled | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Major ChlorproMAZINE Hydrochloride Tablets recalled | The Harvard Drug Group | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Tri-Immune for Injection, all strengths and presentations recalled | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | L-Arginine for Injection, all strengths and presentations recalled | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Taurine for Injection, all strengths and presentations recalled | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Bacteriostatic Water for Injection, all strengths recalled by GenoGenix | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Tirzepatide, 60mg/ for Injection vial lyophilized recalled by GenoGenix | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Tesamorelin for Injection, 15mg Multi-Dose Vial, GenoGenix recalled | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Amino Blend for Injection, all strengths and presentations recalled | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Calcium Chloride for Injection, all strengths recalled by GenoGenix | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Biotin for Injection, all strengths and presentations recalled | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Lysine for Injection, all strengths and presentations recalled | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Norgestimate and Ethinyl Estradiol Tablets recalled by AvKARENorgestimate And Ethinyl Estradiol | AvKARE | Other | Nationwide |
| Drug | CLASS II | Methylene Blue for Injection, all strengths recalled by GenoGenix | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | NAD+ (Nicotinamide adenine dinucleotide), a) 50 mg/mL recalled | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | N-Acetyl-L-Cysteine for Injection, all strengths recalled by GenoGenix | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | L-Carnitine for Injection, all strengths and presentations recalled | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Cerebrolysin for Injection, all strengths and presentations recalled | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Magnesium Chloride for Injection, all strengths recalled by GenoGenix | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | GHK-Cu (Copper Peptide) for Injection, all strengths recalled | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Glycine for Injection, all strengths and presentations recalled | GenoGenix | Sterility | Nationwide |
| Drug | CLASS II | Reconstitution XO Solution for Injection, all strengths recalled | GenoGenix | Sterility | Nationwide |
| Food | CLASS I | Fresh Creative Foods Cooked Farfalle Pasta lb recalled | Nate's Fine Foods | Listeria | 4 states |
| Food | CLASS I | Taylor Farms Cooked Farfalle Map lb recalled by Nate's Fine FoodsTaylor | Nate's Fine Foods | Listeria | 4 states |
| Food | CLASS II | El Rojo Pasta De Harina, Wheat Pellets recalled by El Rojo WholesaleEl Rojo | El Rojo Wholesale | Lead & Heavy Metals | MN |
| Food | CLASS II | Lifted Made-Lemon, Chewable tablet recalled by Eden¿¿¿s ElixirsLifted Made-Lemon | Eden¿¿¿s Elixirs | Undeclared Allergens | TX |
| Food | CLASS II | Toto S'Mores Ooey Gooey Cookie recalledToto S'Mores | Toto Foods | Other | 14 states |
| Food | CLASS II | Gluta Plus (Glutathione)/container recalled by New Spirit NaturalsGluta Plus | New Spirit Naturals | Undeclared Milk | CA |
| Food | CLASS I | Cinnamon Texas Toast recalled by Harris TeeterHarris Teeter | Harris Teeter | Undeclared Milk | 8 states |
| Food | CLASS II | Meal In A Glass protein powder recalled by New Spirit NaturalsMeal | New Spirit Naturals | Undeclared Milk | CA |
| Food | CLASS III | Scott & Jon s Honey Sesame Salmon Rice Bowl recalledScott | Demers Food Group | Undeclared Wheat & Gluten | 9 states |
| Food | CLASS I | Cooked Linguine Pasta Pouches Perishable Keep Refrigerated recalled | Nate's Fine Foods | Listeria | 4 states |
| Food | CLASS I | Taylor Farms Cooked Trotolle Map recalled by Nate's Fine FoodsTaylor | Nate's Fine Foods | Listeria | 4 states |
| Food | CLASS II | Organic BABY bedtime drops recalled by M.O.M Enterprises | M.O.M Enterprises | Mold | 33 states |
| Food | CLASS II | Lifted Made Mint flavored tablets 20mg 7OH/550mg Tablet recalledLifted Made | Eden¿¿¿s Elixirs | Undeclared Allergens | TX |
| Food | CLASS III | G&L Food Dried Bean Curd recalled by Gansu Zhaofeng AgriculturalG&l | Gansu Zhaofeng Agricultural Development Co | Undeclared Allergens | CA |
| Food | CLASS I | Cooked Linguine Pasta lb recalled by Nate's Fine Foods | Nate's Fine Foods | Listeria | 4 states |
| Food | CLASS II | Ultra Whey Protein Powder recalled by New Spirit NaturalsUltra Whey | New Spirit Naturals | Undeclared Milk | CA |
| Food | CLASS II | Eskay Brands Mint flavored tablets recalled by Eden¿¿¿s ElixirsEskay Brands | Eden¿¿¿s Elixirs | Undeclared Allergens | TX |
| Food | CLASS II | FemiClear Daily Bladder Strength Dietary Supplement recalledFemiClear Daily | Organicare Nature's Science | E. coli | Nationwide |
| Food | CLASS I | Kirkland Signature Ahi Tuna Wasabi Poke, Costco #17193 recalledKirkland Signature | Western United Fish Company | Listeria | 37 states |
| Food | CLASS I | Signature Enoki Mushroom recalled by New Age InternationalSignature | New Age International | Listeria | NY |
| Food | CLASS I | Taylor Farms Cooked Rotini Map lb recalled by Nate's Fine FoodsTaylor | Nate's Fine Foods | Listeria | 4 states |
| Food | CLASS I | Asiago Texas Toast recalled by Harris TeeterHarris Teeter | Harris Teeter | Undeclared Milk | 8 states |
| Food | CLASS II | Super Muscle Support Powder;/container recalled by New Spirit NaturalsSuper Muscle | New Spirit Naturals | Undeclared Milk | CA |
| Food | CLASS I | Map Cooked Fettuccine Pasta lbs recalled by Nate's Fine FoodsMap | Nate's Fine Foods | Listeria | 4 states |
| Food | CLASS I | o Nagatoshi Large AA Brown Omega-3 1 dozen cartons o Nijiya recalled | Country Eggs | Salmonella | CA, NV |
| Food | CLASS I | Fresh Creative Foods Cooked Penne Pasta lb recalled by Nate's Fine Foods | Nate's Fine Foods | Listeria | 4 states |
| Food | CLASS I | Cooked Fettuccine Pasta lbs recalled by Nate's Fine Foods | Nate's Fine Foods | Listeria | 4 states |
| Food | CLASS II | Sadecki Bartnik Pylek Kwiatowy (Bee Pollen) glass recalledSadecki Bartnik | Gospodarstwo Pasieczne Sadecki Bartnik | Foreign Material | IL |
| Food | CLASS I | Pinocchio Catering Aged Kimchi Mackerel;; black bottomed recalledPinocchio Catering | Lee K of NY | Undeclared Milk | NJ, NY |
| Food | CLASS II | Taproom Gourmet brand bulk "Empire" Mix recalledTaproom | Egress Capital Partners | Undeclared Allergens | 6 states |
| Food | CLASS II | Taproom Gourmet brand bulk "Park" Mix recalledTaproom | Egress Capital Partners | Undeclared Allergens | 6 states |
| Food | CLASS II | Taproom Gourmet brand bulk "Broadway" Mix recalledTaproom | Egress Capital Partners | Undeclared Allergens | 6 states |
| Food | CLASS II | Taproom Gourmet brand bulk "Madison" Mix recalledTaproom | Egress Capital Partners | Undeclared Allergens | 6 states |
| Food | CLASS II | Taproom Gourmet brand and bulk "Fifth Avenue" Mix recalledTaproom | Egress Capital Partners | Undeclared Allergens | 6 states |
| Device | CLASS II | NES Reprocessed OTW Turbo Elite Laser Atherectomy Catheter recalled | Northeast Scientific | Sterility | Nationwide |
| Device | CLASS I | Magnetom Verio Dot recalled by Siemens Medical Solutions USA | Siemens Medical Solutions USA | Packaging Defects | Nationwide |
| Device | CLASS II | Elan 4 Fixed Duraguard Long recalled by Aesculap AG | Aesculap | Labeling Errors | MO |
| Device | CLASS II | Gore Acuseal Vascular Graft recalled by W L Gore & Associates | W L Gore & Associates | Packaging Defects | 51 states |
| Device | CLASS I | Biograph One (DE) recalled by Siemens Medical Solutions USA | Siemens Medical Solutions USA | Packaging Defects | Nationwide |
| Device | CLASS I | Reprocessed ViewFlex Xtra ICE Catheter to visualize cardiac recalled | Medline Industries | Particulate Matter | Nationwide |
| Device | CLASS I | Magnetom Prisma recalled by Siemens Medical Solutions USA | Siemens Medical Solutions USA | Packaging Defects | Nationwide |
| Device | CLASS II | Venclose digiRF Generators recalled by Bard Peripheral Vascular | Bard Peripheral Vascular | Temperature Abuse | Nationwide |
| Device | CLASS I | Magnetom Connectom.X recalled by Siemens Medical Solutions USA | Siemens Medical Solutions USA | Packaging Defects | Nationwide |
| Device | CLASS I | Reprocessed Acuson AcuNav Ultrasound Catheter recalled | Medline Industries | Particulate Matter | Nationwide |
| Device | CLASS II | Allura Xper/10 recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | Implant Epikut Plus Mt16 recalled by S.I.N. Implant System Ltda | S.I.N. Implant System Ltda | Packaging Defects | Nationwide |
| Device | CLASS II | DxC 500 AU Module w/ISE, DxC 500i, With ISE recalled by Beckman Coulter | Beckman Coulter | Potency & Assay | CA |
| Device | CLASS I | Reprocessed Inquiry Steerable Diagnostics Catheter recalled | Medline Industries | Particulate Matter | Nationwide |
| Device | CLASS I | Magnetom Verio Dot Upgrade recalled by Siemens Medical Solutions USA | Siemens Medical Solutions USA | Packaging Defects | Nationwide |
| Device | CLASS II | NES Reprocessed RX Turbo Elite Laser Atherectomy Catheter recalled | Northeast Scientific | Sterility | Nationwide |
| Device | CLASS II | Allura Xper recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | NES Reprocessed RX Turbo Elite Laser Atherectomy Catheter recalled | Northeast Scientific | Sterility | Nationwide |
| Device | CLASS I | Magnetom Cima.X (DE) recalled by Siemens Medical Solutions USA | Siemens Medical Solutions USA | Packaging Defects | Nationwide |
| Device | CLASS II | Allura Xper OR Table recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS I | Sterile Medline Convenience Kits: Major Pack recalled | Medline Industries | Sterility | 4 states |
| Device | CLASS II | NES Reprocessed OTW Turbo Elite Laser Atherectomy Catheter recalled | Northeast Scientific | Sterility | Nationwide |
| Device | CLASS II | Allura Xper FD20/15 OR Table recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | Vitek¿-negative AST Test Kits (Cards) recalled by bioMerieux | bioMerieux | Sterility | NC |
| Device | CLASS II | Cardio Vascular-Allura Centron recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | Allura Xper FD20/20 recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | Artegraft Collagen Vascular Grafts recalled by LeMaitre Vascular | LeMaitre Vascular | Other | Nationwide |
| Device | CLASS II | Allura Xper Biplane recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS I | Atlan A350XL recalled by Draeger | Draeger | Device Malfunction | 25 states |
| Device | CLASS II | Allura Xper CV20 recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS I | Magnetom Skyra fit recalled by Siemens Medical Solutions USA | Siemens Medical Solutions USA | Packaging Defects | Nationwide |
| Device | CLASS II | Allura Xper Biplane OR Table recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | NES Reprocessed OTW Turbo Elite Laser Atherectomy Catheter recalled | Northeast Scientific | Sterility | Nationwide |
| Device | CLASS II | Allura Xper FD10C recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS I | Magnetom Vida Fit recalled by Siemens Medical Solutions USA | Siemens Medical Solutions USA | Packaging Defects | Nationwide |
| Device | CLASS I | Magnetom Vida (DE) recalled by Siemens Medical Solutions USA | Siemens Medical Solutions USA | Packaging Defects | Nationwide |
| Device | CLASS I | Medline Kits: Valve Pack-lf recalled by Medline Industries | Medline Industries | Device Malfunction | Nationwide |
| Device | CLASS I | Magnetom Skyra Fit BioMatrix recalled by Siemens Medical Solutions USA | Siemens Medical Solutions USA | Packaging Defects | Nationwide |
| Device | CLASS I | Reprocessed Webster CS Catheter 10 Electrodes recalled | Medline Industries | Particulate Matter | Nationwide |
| Device | CLASS I | Magnetom Spectra as the following: Magnetom Spectra recalled | Siemens Medical Solutions USA | Packaging Defects | Nationwide |
| Device | CLASS II | Allura Xper FD10 OR Table recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | Change Healthcare Radiology Solutions recalled | Change Healthcare Canada | Device Malfunction | Nationwide |
| Device | CLASS II | Allura Xper FD20/20 OR Table recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | Exeter V40 Stem No recalled by Howmedica Osteonics | Howmedica Osteonics | Packaging Defects | NJ |
| Device | CLASS I | Magnetom Lumina (DE) recalled by Siemens Medical Solutions USA | Siemens Medical Solutions USA | Packaging Defects | Nationwide |
| Device | CLASS I | Sterile Medline Convenience Kits: Extremity Pack recalled | Medline Industries | Sterility | 4 states |
| Device | CLASS II | Allura Xper FD20/10 recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS I | Magnetom Verio recalled by Siemens Medical Solutions USA | Siemens Medical Solutions USA | Packaging Defects | Nationwide |
| Device | CLASS II | Argus PB-3000, Reference Numbers: 1A.701307 recalled by Schiller, Ag | Schiller | Other | Nationwide |
| Device | CLASS II | Getinge 88-Series Washer- Disinfector recalled | Getinge Disinfection Ab | Device Malfunction | Nationwide |
| Device | CLASS II | Allura Xper FD20/15 recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | NES Reprocessed RX Turbo Elite Laser Atherectomy Catheter recalled | Northeast Scientific | Sterility | Nationwide |
| Device | CLASS II | Elan 4 Fixed Duraguard Standard recalled by Aesculap AG | Aesculap | Labeling Errors | MO |
| Device | CLASS II | Allura Xper recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS I | Reprocessed Livewire Steerable Electrophysiology Catheter recalled | Medline Industries | Particulate Matter | Nationwide |
| Device | CLASS I | Atlan A350 recalled by Draeger | Draeger | Device Malfunction | 25 states |
| Device | CLASS II | Zap-x Radiosurgery System recalled by Zap Surgical Systems | Zap Surgical Systems | Device Malfunction | Nationwide |
| Device | CLASS II | Ashvins variant Heyex 2 / Heyex Pacs recalled by MedicalCommunications | MedicalCommunications | Device Malfunction | Nationwide |
| Device | CLASS II | NES Reprocessed OTW Turbo Elite Laser Atherectomy Catheter recalled | Northeast Scientific | Sterility | Nationwide |
| Device | CLASS II | NES Reprocessed RX Turbo Elite Laser Atherectomy Catheter recalled | Northeast Scientific | Sterility | Nationwide |
| Device | CLASS II | Junctional Emergency Treatment Tool (jett) recalled | North American Rescue | Device Malfunction | Nationwide |
| Device | CLASS I | Biograph mMR recalled by Siemens Medical Solutions USA | Siemens Medical Solutions USA | Packaging Defects | Nationwide |
| Device | CLASS I | Magnetom Skyra (DE) recalled by Siemens Medical Solutions USA | Siemens Medical Solutions USA | Packaging Defects | Nationwide |
| Device | CLASS II | Medtronic, Simplera Sensor recalled by Medtronic MiniMed | Medtronic MiniMed | Sterility | CA |
| Drug | CLASS II | Carbamazepine Extended-Release Tablets recalledCarbamazepine | Amerisource Health Services | Potency & Assay | Nationwide |
| Drug | CLASS II | Ketorolac Tromethamine Ophthalmic Solution recalled by ApotexKetorolac Tromethamine | Apotex | Sterility | Nationwide |
| Drug | CLASS II | Entecavir Tablets, USP, 1 mg recalled by Zydus Pharmaceuticals (USA)Entecavir | Zydus Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution recalledBrimonidine Tartrate/timolol Maleate Ophthalmic Solution | Apotex | Sterility | Nationwide |
| Drug | CLASS II | Entecavir Tablets, USP, 0.5 mg recalled by Zydus Pharmaceuticals (USA)Entecavir | Zydus Pharmaceuticals | Potency & Assay | Nationwide |
| Food | CLASS II | Italian Mixed Vanilla Cookies recalled by Gina Marie Bakery | Gina Marie Bakery | Undeclared Tree Nuts | CT |
| Food | CLASS II | Orwashers Soho Sourdough XL Batard recalled by Oven ArtisansOrwashers | Oven Artisans | Undeclared Sesame | MA |
| Food | CLASS I | Cucumbers Sliced 1/4" Cucumber Sliced 1/4" recalled by Chefs WarehouseCucumbers | Chefs Warehouse | Salmonella | DE, MD, VA |
| Food | CLASS II | 16/25 Frozen Cooked Tail-On Farm Raised Shrimp recalled | Lawrence Wholesale | Foreign Material | 16 states |
| Food | CLASS I | Cucumber Diced 1/2" recalled by Chefs Warehouse | Chefs Warehouse | Salmonella | DE, MD, VA |
| Food | CLASS III | Toasted Almond & Cherry Biscotti recalled by Gina Marie Bakery | Gina Marie Bakery | Undeclared Allergens | CT |
| Food | CLASS III | Nafco, Whiting Fillet Skin-on Boneless Iqf, Cases are corrugate recalledNafco | Stanley Pearlman Enterprises | Other | MD, PA |
| Food | CLASS II | vitamins B12 dietary supplement Raspberry Flavored sold recalledfollowing | Vitalabs | Undeclared Peanuts | IL, NJ |
| Food | CLASS III | Vanilla Chocolate Dipped Cookies recalled by Gina Marie Bakery | Gina Marie Bakery | Undeclared Allergens | CT |
| Food | CLASS II | Lipton Green Tea Citrus recalled by PepsicoLipton | Pepsico | Undeclared Allergens | 10 states |
| Food | CLASS II | Vanilla with Apricot Jam Cookies recalled by Gina Marie Bakery | Gina Marie Bakery | Undeclared Allergens | CT |
| Food | CLASS II | Shrimp Cocktail Bowl recalled by Lawrence Wholesale | Lawrence Wholesale | Foreign Material | 16 states |
| Food | CLASS I | Cucumbers Diced 1/4" recalled by Chefs WarehouseCucumbers Diced | Chefs Warehouse | Salmonella | DE, MD, VA |
| Food | CLASS I | 98 cs Cucumber - Super recalled by Chefs Warehouse | Chefs Warehouse | Salmonella | DE, MD, VA |
| Food | CLASS I | 190 cs Cucumber Select recalled by Chefs Warehouse | Chefs Warehouse | Salmonella | DE, MD, VA |
| Food | CLASS II | Italian Sesame Cookies recalled by Gina Marie Bakery | Gina Marie Bakery | Undeclared Sesame | CT |
| Food | CLASS II | Frozen Raw Easy Peel shrimp, IQF bag/case recalled by Tas Tematic Foods | Tas Tematic Foods | Other | CA |
| Food | CLASS III | Toasted Cherry Biscotti recalled by Gina Marie Bakery | Gina Marie Bakery | Undeclared Allergens | CT |
| Food | CLASS I | Whole Foods Market Blueberry Almond Granola recalled by WFM Purchasing | WFM Purchasing | Undeclared Wheat & Gluten | PA |
| Food | CLASS II | Vanilla Cookies with Raspberry Peach Jam recalled by Gina Marie Bakery | Gina Marie Bakery | Undeclared Allergens | CT |
| Food | CLASS I | Der Mutterschaf Cheese, Sheep Tomme Style recalled by Goot EssaGoot Essa | Goot Essa | Listeria | 4 states |
| Food | HEALTH ALERT | Ready-To-Eat Meals Containing Riced Cauliflower recalled | Freshrealm FreshRealm | Listeria | |
| Food | HEALTH ALERT | Ready-To-Eat Meals Containing Spinach recalled by FreshRealm, FreshRealm | FreshRealm, FreshRealm, FreshRealm | Listeria | |
| Food | CLASS I | Chicken Corn Dog and Ground Turkey on a Stick Products recalled | Foster Poultry Farms | Foreign Material | |
| Device | CLASS II | Allura Xper FD20/10 recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | Philips CT systems labeled as the following: Brilliance iCT SP recalled | Philips North America | Other | Nationwide |
| Device | CLASS II | Allura Xper FD20/20 recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | Allura Xper recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | Philips CT systems labeled as the following recalled | Philips North America | Other | Nationwide |
| Device | CLASS II | Stratafix Spiral PDS Plus Bidirectional Knotless Tissue recalled | Ethicon | Other | Nationwide |
| Device | CLASS II | Sofmed Breathables, (stenfilcon A) contact lens recalled by CooperVision | CooperVision | Sterility | Nationwide |
| Device | CLASS I | Medline medical convenience kits labeled as recalled | Medline Industries LP - Northfield | Device Malfunction | 6 states |
| Device | CLASS II | Extractor Pro RX Retrieval Balloon Catheter recalled | Boston Scientific | Labeling Errors | Nationwide |
| Device | CLASS II | Philips CT systems labeled as the following: Ingenuity CT recalled | Philips North America | Other | Nationwide |
| Device | CLASS II | Voyant 1-Day Premium Toric, (stenfilcon A) contact lens recalled | CooperVision | Sterility | Nationwide |
| Device | CLASS II | Philips CT systems labeled as the following recalled | Philips North America | Other | Nationwide |
| Device | CLASS II | BeneVision N1 Patient Monitor (N1) recalled by Mindray DS USA | Mindray DS USA | Device Malfunction | Nationwide |
| Device | CLASS II | Allura Xper Biplane OR Table recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | FilmArray Ngds Warrior Panel Ngds-asy-0007 is a qualitative recalled | Biofire Defense | Device Malfunction | Nationwide |
| Device | CLASS II | Juggerknot Mini Soft Anchors recalled by Biomet | Biomet | Other | Nationwide |
| Device | CLASS II | Philips CT systems labeled as the following: Brilliance 16 Power recalled | Philips North America | Other | Nationwide |
| Device | CLASS II | Allura Xper FD20/20 OR Table recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | Philips CT systems labeled as the following: CT recalled | Philips North America | Other | Nationwide |
| Device | CLASS II | MyDay Toric, stenfilcon A) Contact Lens recalled by CooperVision | CooperVision | Sterility | Nationwide |
| Device | CLASS II | Allura Xper OR Table recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | Allura Xper recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | Philips CT systems labeled as the following recalled | Philips North America | Other | Nationwide |
| Device | CLASS II | Philips CT systems labeled as the following: Big Bore RT recalled | Philips North America | Other | Nationwide |
| Device | CLASS II | Ortoma Inserter Adapter OTD: Inserter Adapter OTD Straight recalled | Ortoma AB | Device Malfunction | Nationwide |
| Device | CLASS II | Philips CT systems labeled as the following: IQon Spectral CT recalled | Philips North America | Other | Nationwide |
| Device | CLASS II | Allura CV20 recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | Philips CT systems labeled as the following: Brilliance iCT recalled | Philips North America | Other | Nationwide |
| Device | CLASS II | Chromophare Surgical Light System recalled by Stryker Communications | Stryker Communications | Other | Nationwide |
| Device | CLASS I | Automated Impella Controller (AIC) with the below brands recalled | Abiomed | Device Malfunction | 17 states |
| Device | CLASS II | Allura Xper OR Table recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | Vasoview Hemopro 3 Endoscopic Vessel Harvesting System recalled | Maquet Cardiovascular | Device Malfunction | Nationwide |
| Device | CLASS II | Allura Xper FD20/15 OR Table recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS I | Medline medical convenience kits labeled as recalled | Medline Industries LP - Northfield | Device Malfunction | 6 states |
| Device | CLASS II | Allura Xper/10 recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | Allura Xper FD20/15 recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | Allura Xper Biplane recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | t:slim X2 Insulin Pump with Interoperable Technology recalled | Tandem Diabetes Care | Device Malfunction | CA |
| Device | CLASS II | Baster Continu-Flo Solution Set, Non-Vented recalled | Baxter Healthcare | Other | Nationwide |
| Drug | CLASS II | Quick Touch Alcohol Prep Pads(Isopropyl Alcohol 70%) recalled | Yangzhou Yulou Paper Products | Manufacturing (CGMP) Deviations | N/A |
| Drug | CLASS III | Dextroamphetamine Saccharate recalled by Granules PharmaceuticalsDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate | Granules Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Torrey Pines Dermatology & Laser Center Benzaderm BPO recalled | Private Label Skin Care | Benzene | CA, GA |
| Drug | CLASS II | Skin MD by Dr Monika Kiripolsky, Body Acne Cleanser recalled | Private Label Skin Care | Benzene | CA, GA |
| Drug | CLASS III | Readyprep PVP, Povidone-Iodine 10% Solution recalledPovidone-iodine | Medline Industries | Potency & Assay | Nationwide |
| Drug | CLASS II | Micronized BPO Gel Cleanser recalled by Private Label Skin Care | Private Label Skin Care | Benzene | CA, GA |
| Drug | CLASS III | Dextroamphetamine Saccharate recalled by Granules PharmaceuticalsDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate | Granules Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS III | Dextroamphetamine Saccharate recalled by Granules PharmaceuticalsDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate | Granules Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | mel rx Skin, NO Drama Benzoyl Peroxide 10% Acne Treatment recalled | Private Label Skin Care | Benzene | CA, GA |
| Drug | CLASS III | Dextroamphetamine Saccharate recalled by Granules PharmaceuticalsDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate | Granules Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS III | Dextroamphetamine Saccharate recalled by Granules PharmaceuticalsDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate | Granules Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Artisan OF Skin (Benzoyl Peroxide 10%) recalled | Private Label Skin Care | Benzene | CA, GA |
| Drug | CLASS III | Kroger 70% Isopropyl Alcohol recalled by Consumer Product Partners70% Isopropyl Rubbing Alcohol | Consumer Product Partners | Other | Nationwide |
| Drug | CLASS III | TopCare Health 70% Isopropyl Alcohol recalled70% Isopropyl Rubbing Alcohol | Consumer Product Partners | Other | Nationwide |
| Drug | CLASS II | edunn clarity, BP Treatment Cleanser recalled by Private Label Skin Care | Private Label Skin Care | Benzene | CA, GA |
| Drug | CLASS II | Azelaic Acid Gel, 15%, For Topical Use Only recalledAzelaic Acid | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Food | CLASS I | Middlefield Original Cheese Co-op Monterey Jack recalled | Middlefield Original Cheese Cooperative | Listeria | 4 states |
| Food | CLASS II | Dietary Supplement Strength: 20mg CBD recalled by Extract Labsmg Gummies | Extract Labs | Undeclared Allergens | Nationwide |
| Food | CLASS III | Mmbal pasteurized donor human milk (Pdhm) recalledMmbal | Mothers' Milk Bank of Alabama | Foreign Material | AL |
| Food | CLASS III | UDK ,Half Plum, Container, 24, ambient recalled by SUNGALUdk | SUNGAL | Other | 4 states |
| Food | CLASS I | Middlefield Original Cheese Co-op All Natural Mild Cheddar recalled | Middlefield Original Cheese Cooperative | Listeria | 4 states |
| Food | CLASS I | Sunrise Creamery Dilly Pickle Monterey Jack Cheese with Dill Pickles recalled | Middlefield Original Cheese Cooperative | Listeria | 4 states |
| Food | CLASS I | Middlefield Original Cheese Co-op Organic Gouda Cheese recalledMiddlefield | Middlefield Original Cheese Cooperative | Listeria | 4 states |
| Food | CLASS II | Dietary Supplement Strength: 20mg CBD recalled by Extract Labsmg Gummies | Extract Labs | Undeclared Allergens | Nationwide |
| Food | CLASS I | Middlefield Original Cheese Co-op Original Swiss Cheese recalledMiddlefield | Middlefield Original Cheese Cooperative | Listeria | 4 states |
| Food | CLASS I | Middlefield Original Cheese Co-op Shredded recalledMiddlefield | Middlefield Original Cheese Cooperative | Listeria | 4 states |
| Food | CLASS II | Dietary Supplement Strength: 10mg CBD recalled by Extract LabsBerry Gummies | Extract Labs | Packaging Defects | Nationwide |
| Food | CLASS II | Pure Cane Granulated Sugar recalled by Domino Foods | Domino Foods | Foreign Material | CA, UT |
| Food | CLASS I | Goodles Vegan Is Believin' Plant-based White Cheddar With Spirals recalledGoodles | Gooder Foods | Undeclared Allergens | 37 states |
| Food | CLASS I | Middlefield Original Cheese Co-op All Natural Pepper Jack recalled | Middlefield Original Cheese Cooperative | Listeria | 4 states |
| Food | CLASS I | Goodles Here Comes Truffle Creamy Truffle Flavored Cheddar recalledGoodles Here | Gooder Foods | Undeclared Allergens | 37 states |
| Food | CLASS I | Middlefield Original Cheese Co-op Shredded Mozzarella recalledMiddlefield | Middlefield Original Cheese Cooperative | Listeria | 4 states |
| Food | CLASS I | Middlefield Original Cheese Co-op Smoked Cheddar loaves recalledMiddlefield | Middlefield Original Cheese Cooperative | Listeria | 4 states |
| Food | CLASS II | Dietary Supplement Strength: 20mg CBD recalled by Extract Labsmg Gummies | Extract Labs | Undeclared Allergens | Nationwide |