| Device | CLASS II | Ingenia 1.5T CX - Magnetic Resonance recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Achieva 3.0T TX for PET recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Syr L/l Purple Nitro recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | AchievaXR -Magnetic Resonance recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Syr L/l Red recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | GMAX SYR/LL syringe recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medline Syr L/l recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Ingenia 1.5T S recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Immulite 2000 Anti-TG Ab recalled by Siemens Healthcare Diagnostics | Siemens Healthcare Diagnostics | Other | Nationwide |
| Device | CLASS II | Medline Syr L/l White Saline recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Noblus AC Adapter used with the Noblus Ultrasound Imaging System recalled | Fujifilm Healthcare Americas | Other | Nationwide |
| Device | CLASS II | Medline Syr L/l Yellow Cont recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Incisive CT - Computed Tomography X-Ray System intended recalled | Philips North America | Foreign Material | Nationwide |
| Device | CLASS II | Immulite 2000 Anti-TG Ab recalled by Siemens Healthcare Diagnostics | Siemens Healthcare Diagnostics | Other | Nationwide |
| Device | CLASS II | Yamaha Surface Mounter YR series, YS series, i-Pulse series recalled | Yamaha Motor | Other | Nationwide |
| Device | CLASS II | Medline Syr L/l Red Lido recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | GMAX SYR/LL Blue syringe recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medline Syr L/l Green recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | SmartPath to Ingenia Elition X - Magnetic Resonance recalled | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Syr L/l White recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medline Syr L/l Blue recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | GMAX SYR/LL syringe recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Incisive CT - Computed Tomography X-Ray System intended recalled | Philips North America | Foreign Material | Nationwide |
| Device | CLASS II | SmartPath to dStream for XR and 3.0T- Magnetic Resonance recalled | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Ingenia 1.5T recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Upgrade dStream - Magnetic Resonance recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Syr L/l Blue Saline recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Wolf Medical - Wolf-pak Disposable Syringe recalled | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | GMAX SYR/LL syringe recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Achieva 1.5T Conversion- Magnetic Resonance recalled | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Syr L/l Yellow recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medline Syr L/l Blue recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | SmartPath to dStream for 1.5T- Magnetic Resonance recalled | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Surgifoam" Absorbable Gelatin Powder Kit, Product recalled by Ethicon | Ethicon | Packaging Defects | Nationwide |
| Device | CLASS II | Ingenia 3.0T CX recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Optical Inspection System, YSi series, YRi series recalled | Yamaha Motor | Processing Deviation | Nationwide |
| Device | CLASS II | Marlin 1.5T - Magnetic Resonance recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Syr L/l Control recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Achieva 3.0T for PET -Magnetic Resonance recalled | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Syr L/l Blue Heparin recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medline Syr/ls recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medline Syr/l Blue Contrast recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medline Syr L/l Purple recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | InstaClear Lens Sheath recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Syr L/l Yellow Nitro recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medline Syr L/s recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Cerene Cryotherapy Device, Thermal Ablation, Endometrial recalled | Channel Medsystems | Other | Nationwide |
| Device | CLASS II | Ingenia 3.0T- Magnetic Resonance recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Wolf Medical (cc) Luer Lock Sterile Latex Free Non Pyrogenic recalled | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Panorama HFO- Magnetic Resonance recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Syr L/s Blue recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | GMAX SYR/LL syringe recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medline Syr L/l Red Nitro recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medline Syr L/l Yellow recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Achieva 1.5T- Magnetic Resonance recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | GMAX SYR/LS syringe recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Wolf Medical (cc) Luer Lock Sterile Latex Free Non Pyrogenic recalled | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | GMAX SYR/LS syringe recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Wolf Medical (cc) Luer Lock Sterile Latex Free Non Pyrogenic recalled | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medline Syr L/l White recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | GMAX SYR/LL syringe recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Ingenia Elition X- Magnetic Resonance recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Syr L/l Green recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medline Syr L/s recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Wolf Medical (cc) Luer Lock Sterile Latex Free Non Pyrogenic recalled | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | GMAX SYR/LS syringe recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | 8000-021-002, Scopis¿ ENT recalled by Stryker Leibinger GmbH & Co. | Stryker Leibinger GmbH & Co. KG | Device Malfunction | Nationwide |
| Device | CLASS II | MR RT - Magnetic Resonance (MR) systems are Medical recalled | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Syr L/l Purple recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | GMAX SYR/LL syringe recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Achieva 1.5T Initial system recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Syr L/l Blue Lido recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Intera 1.5T- Magnetic Resonance recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Syr L/l recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | GMAX SYR/LL syringe recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Sonalleve MR HIFU 3.0T - Magnetic Resonance recalled | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Syr L/s White Lido recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medline Syr L/l Yellow Lido recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medline Syr L/l recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medline Syr L/l Red recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medline Syr L/l recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Stryker Blueprint recalled by Tornier S.A.S | Tornier S.A.S | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Syr L/l Blue recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medigrative 100cc/ml disposable luer lock syringe recalled | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medline Syr Tb recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medline Syr L/s recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medline Syr L/l Yellow Lido recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medline Syr L/s Red recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | MR RT Upgrades- Magnetic Resonance recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Cascade Iomax Cortical Module recalled by Cadwell Industries | Cadwell Industries | Other | Nationwide |
| Device | CLASS II | Medline Syr L/l recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medline Syr L/l Red recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | MR 5300- Magnetic Resonance recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Syr Cntrl L/l Blue recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | 2008T BlueStar Hemodialysis Machine recalled by Fresenius Medical Care | Fresenius Medical Care Holdings | Other | Nationwide |
| Device | CLASS II | Medline Syr Cntrl L/l Yellow Lido recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS I | Optum Nimbus II Plus recalled by OptumHealth Care Solutions | OptumHealth Care Solutions | Packaging Defects | Nationwide |
| Device | CLASS II | Medline Syr L/l Green Cont recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Evolution upgrade 1.5T- Magnetic Resonance recalled | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | 2008T BlueStar Hemodialysis Machine recalled by Fresenius Medical Care | Fresenius Medical Care Holdings | Other | Nationwide |
| Device | CLASS II | Medline Syr L/l Red Cont recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Prelude Guide Sheath Roadster recalled by Merit Medical Systems | Merit Medical Systems | Other | Nationwide |
| Device | CLASS II | Medline Syr L/l Blue recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medline Syr Cntrl L/l Green recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medline Syr L/s recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medline Syr/l White Hep Flush recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | GMAX SYR/LL syringe recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medline Syr L/l Red Heparin recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medline Syr/l Purple recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medline Syr/l White Contrast recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medline Syr Cntr L/l Yellow recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | GMAX SYR/LL Blue syringe recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Wolf Medical (cc) Luer Lock Sterile Latex Free Non Pyrogenic recalled | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medline Syr L/l Yellow Hep/saline recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | GMAX SYR Control syringe recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | GMAX SYR/LS syringe recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medline Syr L/l White recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medline Syr L/l Blue Saline recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Integra¿ Cranial access kit recalled by Integra LifeSciences | Integra LifeSciences | Sterility | Nationwide |
| Device | CLASS II | Evolution upgrade 3.0T recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | SmartPath to dStream for 3.0T recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Ingenia Ambition X- Magnetic Resonance recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Ingenia Ambition S recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Syr L/l Green recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | MR system 1.5T Marlin- Magnetic Resonance recalled | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Blood Pump Rotor recalled by Fresenius Medical Care | Fresenius Medical Care Holdings | Other | Nationwide |
| Device | CLASS II | Medline Syr L/l Yellow recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medline Syr Cntrl L/l Red recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Prelude Guide Sheath Roadster recalled by Merit Medical Systems | Merit Medical Systems | Other | Nationwide |
| Device | CLASS II | Medline Syr L/s recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Wolf Medical (cc) Luer Lock Sterile Latex Free Non Pyrogenic recalled | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Achieva 3.0T recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | GMAX SYR/LL syringe recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medline Syr L/l Purple recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medline Syr L/l Red recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | Medline Syr L/l Green recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Device | CLASS II | GMAX SYR/LL syringe recalled by Jiangsu Shenli Medical | Jiangsu Shenli Medical Production | Other | Nationwide |
| Drug | CLASS II | niCARdipine Hydrochloride Injection, USP, 25 mg recalledNicardipine Hydrochloride | American Regent | Sterility | UT |
| Drug | CLASS II | Duloxetine Delayed-Release Cap USP 30mg recalled | Preferred Pharmaceuticals | Nitrosamine Impurity | 5 states |
| Drug | CLASS II | Vasopressin Injection, USP per mL) Multiple-Dose Vial recalledVasopressin | American Regent | Potency & Assay | Nationwide |
| Drug | CLASS III | Xelpros (latanoprost ophthalmic emulsion) 0.005%, 125mcg recalledXelpros | SUN Pharmaceutical Industries | Particulate Matter | PA, TX |
| Drug | CLASS I | Phenylephrine in 0.9% Sodium Chloride Injection recalled | Hikma Injectables USA | Labeling Errors | 5 states |
| Drug | CLASS II | Haloperidol decanoate Injection 50mg/mL recalledHaloperidol Decanoate | Somerset Therapeutics | Foreign Material | Nationwide |
| Drug | CLASS III | Sirolimus Tablets 1mg Tablets recalled by Dr. Reddy's LaboratoriesSirolimus | Dr. Reddy's Laboratories | Potency & Assay | Nationwide |
| Food | CLASS I | Queso de mano, Fresh soft white cheese recalled by TamaQueso | Tama | Listeria | UT |
| Food | CLASS II | Amyloid Complete recalled by FoodScienceAmyloid Complete | FoodScience | Undeclared Fish & Shellfish | 5 states |
| Food | CLASS I | Sammy's Milk Goat Milk Toddler Formula recalled by GraceleighSammy's | Graceleigh | Processing Deviation | 43 states |
| Food | CLASS II | Price Chopper Fat Free Cottage Cheese with Pineapple Added recalledPrice Chopper | HP Hood (LAFARGEVILLE) | Undeclared Allergens | NY |
| Food | CLASS III | chuao Chocolatier potato chip mini chocolate bar recalled | Kairo's Group | Undeclared Tree Nuts | 44 states |
| Food | CLASS I | Spicy Salmon Ingredients read in part: "***Ingredients:Rice recalledGeissler's Supermarket | Geissler's Supermarket | Undeclared Allergens | CT, MA |
| Food | CLASS I | Shrimp Tempura and Spicy Shrimp Ingredients read in part recalledGeissler's Supermarket | Geissler's Supermarket | Undeclared Allergens | CT, MA |
| Food | CLASS I | Sammy's Milk Goat Milk Toddler Formula Stick Pak recalled by GraceleighSammy's | Graceleigh | Processing Deviation | 43 states |
| Food | CLASS I | Pink Lady Salmon &Avo Roll Combo recalled by Geissler's SupermarketGeissler's Supermarket | Geissler's Supermarket | Undeclared Allergens | CT, MA |
| Food | CLASS II | Wegman's Half Loaf Garlic Bread recalled by Wegmans Food MarketsWegman's Half | Wegmans Food Markets | Undeclared Milk | NY, PA |
| Food | CLASS II | Marketside Brioche Rolls, Authentic French Recipe recalledMarketside Brioche | Bakerly Barn | Undeclared Soy | AR |
| Food | CLASS II | Tiramisu Italian Dessert, 2 trays recalled by Mucci Food ProductsMucci | Mucci Food Products | Undeclared Milk | MI |
| Food | CLASS II | Supreme Tradition and Marcum brand ground cinnamon recalledSupreme Tradition | Colonna Brothers | Lead & Heavy Metals | Nationwide |
| Food | CLASS II | Product is Macaroni Salad, but the bottom container recalledProduct | Reser's Fine Foods | Undeclared Wheat & Gluten | 15 states |
| Food | CLASS I | Spicy Tuna Ingredients read in part: "***Ingredients: Rice recalledGeissler's Supermarket | Geissler's Supermarket | Undeclared Allergens | CT, MA |
| Food | CLASS II | Bulk flour tortillas sold to food service recalledBulk | La Original Tortilla Co | Undeclared Wheat & Gluten | TX |
| Food | CLASS I | Shrimp Tempura and Lobster Roll recalled by Geissler's SupermarketGeissler's Supermarket | Geissler's Supermarket | Undeclared Allergens | CT, MA |
| Food | CLASS II | YoCrunch¿ Vanilla Lowfat Yogurt with M&Ms 18 cups recalled by Danone UsYoCrunch | Danone Us | Undeclared Wheat & Gluten | FL |
| Food | CLASS III | Fiji Natural Artesian Water Case recalled by Natural Waters of VitiFiji | Natural Waters of Viti | Other | Nationwide |
| Food | CLASS II | Philadelphia Avo or Cucumber Classic Roll recalledGeissler's Supermarket | Geissler's Supermarket | Undeclared Allergens | CT, MA |
| Device | CLASS II | Medtronic Venous Cannulae: a) DLP¿. Malleable Single Stage recalled | Medtronic Perfusion Systems | Sterility | MN |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS II | Medtronic Arterial Cannulae packaged as recalled | Medtronic Perfusion Systems | Sterility | MN |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS II | EchoTip¿ Ultra Endoscopic Ultrasound Access Needle, Echo-19, G31520 recalled | Cook Medical | Other | IN |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS II | Vitros Immunodiagnostic Products Free T3 Reagent Pack-IVD recalled | Quidelortho | Other | Nationwide |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS II | Medtronic Aortic Root Cannulae and Cardioplegia Needles recalled | Medtronic Perfusion Systems | Sterility | MN |
| Device | CLASS II | Spectrum IQ Infusion pump, Product recalled by Baxter Healthcare | Baxter Healthcare | Device Malfunction | Nationwide |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS II | Reagent Test Strips for Blood, Urobilinogen, Bilirubin recalled | Macherey Nagel Gmbh & Co. Kg | Other | Nationwide |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS II | CardinalHealth Curity Flexible Adhesive Bandage X-Large recalled | Cardinal Health 200 | Labeling Errors | Nationwide |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS II | Sterile CoFlex NL: Latex Free Flexible Cohesive Bandage recalled | Andover Healthcare | Sterility | Nationwide |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS II | Medtronic Clearview Blower/Mister recalled | Medtronic Perfusion Systems | Sterility | MN |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS II | Vitros Immunodiagnostic Products Free T3 Calibrators-IVD recalled | Quidelortho | Other | Nationwide |
| Device | CLASS II | WishFIX Growth Control Plating System recalled by Wishbone Medical | Wishbone Medical | Packaging Defects | CT, FL, NJ |
| Device | CLASS II | Airvo 2 Humidifier recalled by Fisher & Paykel Healthcare | Fisher & Paykel Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Threaded IM Nail, TI recalled by TriMed | TriMed | Potency & Assay | Nationwide |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS II | Laser Application Instrument recalled by Karl Storz Endoscopy | Karl Storz Endoscopy | Sterility | Nationwide |
| Device | CLASS II | Medtronic Tourniquet Sets: a) DLP¿ Tourniquet Kit recalled | Medtronic Perfusion Systems | Sterility | MN |
| Device | CLASS II | RKN130003, Rheo Knee 3 YR Warranty, MD, CE recalled by Ossur H / F | Ossur H / F | Other | Nationwide |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS II | EchoTip¿ Ultra HD Endoscopic Ultrasound Access Needle recalled | Cook Medical | Other | IN |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS II | Medtronic I.M.A recalled by Medtronic Perfusion Systems | Medtronic Perfusion Systems | Sterility | MN |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS II | Ingenia 3.0T with Evolution Upgrade 3.0T recalled | Philips North America | Temperature Abuse | Nationwide |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS II | Threaded IM Nail, TI recalled by TriMed | TriMed | Potency & Assay | Nationwide |
| Device | CLASS II | RKNXC0003, Rheo Knee XC 3 YR Warranty, MD, CE recalled by Ossur H / F | Ossur H / F | Other | Nationwide |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS II | Medtronic Suction Tubes: a) DLP¿ Suction Tube 6-Fr recalled | Medtronic Perfusion Systems | Sterility | MN |
| Device | CLASS II | Medtronic DLP Coronary Ostial Cannulae recalled | Medtronic Perfusion Systems | Sterility | MN |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS II | Pressio¿ Ventricular Intracranial Pressure Monitoring Kit recalled | Sophysa | Packaging Defects | Nationwide |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS II | Syntel Silicone Thrombectomy Catheter, Sterile recalled | LeMaitre Vascular | Other | Nationwide |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS II | namic Convenience Kit, a) Carotid Manifold Kit recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS II | Aptus 2.8 TriLock Screw, HD7, 1/Pkg recalled by Medartis | Medartis | Foreign Material | Nationwide |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS II | RKNXC0005, Rheo Knee XC 5 YR Warranty, MD, CE recalled by Ossur H / F | Ossur H / F | Other | Nationwide |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS II | HeartSine samaritan PAD (Public Access Defibrillator), Type recalled | HeartSine Technologies | Other | Nationwide |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS II | Medtronic Cardioplegia Adapters: a) DLP¿ 1.8 m recalled | Medtronic Perfusion Systems | Sterility | MN |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS II | Novalung sensor box is a component of the Novalung Console recalled | Fresenius Medical Care Holdings | Device Malfunction | Nationwide |
| Device | CLASS II | Namic Fluid Delivery Set recalled by MEDLINE INDUSTRIES, LP | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | RKN130002, Rheo Knee 2 YR Warranty, MD, CE recalled by Ossur H / F | Ossur H / F | Other | Nationwide |
| Device | CLASS II | Medtronic Left Heart Vent Catheters: a) DLP¿ Intracardiac Sump recalled | Medtronic Perfusion Systems | Sterility | MN |
| Device | CLASS II | Medtronic Intracoronary Shunts: a) ClearView¿ Intracoronary Shunt recalled | Medtronic Perfusion Systems | Sterility | MN |
| Device | CLASS II | Patient Information Center iX recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS II | Pressio¿ Ventricular Intracranial Pressure Monitoring Kit recalled | Sophysa | Packaging Defects | Nationwide |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS II | Medtronic Vessel Cannulae: a) DLP¿ Vessel Cannula Blunt Tip recalled | Medtronic Perfusion Systems | Sterility | MN |
| Device | CLASS II | Ingenia 1.5T with Evolution Upgrade 1.5T recalled | Philips North America | Temperature Abuse | Nationwide |
| Device | CLASS I | Expo 5F Selective Angiographic Catheters recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS II | Medtronic Disposable Pressure Display Sets: a) DLP¿ recalled | Medtronic Perfusion Systems | Sterility | MN |
| Device | CLASS II | Cardiohelp-i System recalled by Maquet Medical Systems U | Maquet Medical Systems USA | Packaging Defects | Nationwide |
| Drug | CLASS II | Cefdinir for Oral Suspension USP 125 mg/ when reconstituted) recalledCefdinir | Lupin Pharmaceuticals | Foreign Material | Nationwide |
| Drug | CLASS II | Losartan Potassium and Hydrochlorothiazide Tablets recalledLosartan Potassium And Hydrochlorothiazide | Macleods Pharma USA | Foreign Material | Nationwide |
| Drug | CLASS II | CVS Health Magnesium Citrate Saline Laxative Oral Solution recalledMagnesium Citrate | Pharma Nobis | Sterility | Nationwide |
| Drug | CLASS II | Meijer Magnesium Citrate Saline Laxative Oral Solution Dye recalledMagnesium Citrate | Pharma Nobis | Sterility | Nationwide |
| Drug | CLASS I | Schwinnng Herbal Dietary Supplement Capsules recalled by Stop Clopez | Stop Clopez | Packaging Defects | FL |
| Drug | CLASS II | MethylPREDNISolone Acetate Injectable Suspension recalledMethylprednisolone Acetate | Sagent Pharmaceuticals | Particulate Matter | Nationwide |
| Drug | CLASS II | Gordofilm Wart Remover (salicylic acid 16.7% USP) recalled | Dercher Enterprises Inc | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Cefdinir for Oral Suspension USP 250 mg/ when reconstituted) recalledCefdinir | Lupin Pharmaceuticals | Foreign Material | Nationwide |
| Food | CLASS I | Organic Basil recalled by Infinite HerbsInfinite Herbs | Infinite Herbs | Salmonella | 7 states |
| Food | CLASS I | Sensible Portions Garden Veggie Straws Sea Salt recalledSensible Portions | The Hain Celestial Group | Undeclared Milk | 9 states |
| Food | CLASS II | Jalapenos packed in 6lb 10oz cans. 6 cans per case recalledJalapenos | M-C McLANE INTERNATIONAL | Foreign Material | 28 states |
| Food | CLASS III | Organic Yogi Echinacea Immune Support recalled by East West Tea Company | East West Tea Company | Other | Nationwide |
| Food | CLASS II | Savor Spicy Mango slices recalled by Savor Fine FoodsSavor | Savor Fine Foods | Undeclared Soy | 5 states |
| Food | CLASS III | Country Club, Price Chopper, Good & Gather, Hiland recalled | Hiland Dairy Foods Company | Other | KS, MO |
| Food | CLASS II | Sysco Classic Riced Cauliflower recalled by CN Frozen FoodsSysco | CN Frozen Foods | Listeria | TX |
| Device | CLASS II | Duramax Stacked Tip Straight Vasc-pak recalled by Angiodynamics | Angiodynamics | Other | VA |
| Device | CLASS II | Stryker Dynamic Mesh- Std-medium-Intended recalled | Stryker Leibinger GmbH & Co. KG | Labeling Errors | Nationwide |
| Device | CLASS I | Stealth S8 Clinical recalled by Medtronic Navigation | Medtronic Navigation | Device Malfunction | Nationwide |
| Device | CLASS II | Baxter Spectrum IQ Infusion Pump, Product recalled by Baxter Healthcare | Baxter Healthcare | Other | Nationwide |
| Device | CLASS II | Duramax Stacked Tip Str recalled by Angiodynamics | Angiodynamics | Foreign Material | VA |
| Device | CLASS II | GE Healthcare Allia IGS 5 Pulse recalled by GE Medical Systems, SCS | GE Medical Systems SCS | Other | Nationwide |
| Device | CLASS II | 5000 Compact Series Ultrasound Systems, Product recalled | Philips Ultrasound | Temperature Abuse | Nationwide |
| Device | CLASS II | GE Healthcare Innova IGS 6, Interventional fluoroscopic recalled | GE Medical Systems SCS | Other | Nationwide |
| Device | CLASS II | Duraflow 2 Straight Basic Kit, 1 per Bx Pg-Indicated recalled | Angiodynamics | Foreign Material | VA |
| Device | CLASS II | GE Healthcare Allia IGS 7, Interventional fluoroscopic x-ray systems recalled | GE Medical Systems SCS | Other | Nationwide |
| Device | CLASS II | GE Healthcare Innova IGS 5, computed tomography x-ray system recalled | GE Medical Systems SCS | Other | Nationwide |
| Device | CLASS II | Duraflow 2 Straight Vasc-pak PG- Indicated for use recalled | Angiodynamics | Foreign Material | VA |
| Device | CLASS II | GE Healthcare Allia IGS 5 Pulse recalled by GE Medical Systems, SCS | GE Medical Systems SCS | Other | Nationwide |
| Device | CLASS II | Duramax Stacked Tip Str recalled by Angiodynamics | Angiodynamics | Foreign Material | VA |
| Device | CLASS II | Clinical Chemistry Calibration Serum recalled by Randox Laboratories | Randox Laboratories | Other | Nationwide |
| Device | CLASS II | Duraflow 2 Straight Vasc-pak PG- Indicated for use recalled | Angiodynamics | Foreign Material | VA |
| Device | CLASS II | Duramax Stacked Tip Straight Vasc-pak recalled by Angiodynamics | Angiodynamics | Foreign Material | VA |
| Device | CLASS I | t:connect mobile app used in conjunction recalled | Tandem Diabetes Care | Device Malfunction | Nationwide |
| Device | CLASS II | Duramax Stacked Tip Straight Vasc-pak recalled by Angiodynamics | Angiodynamics | Foreign Material | VA |
| Device | CLASS II | Perla Tl 25d Screw recalled by Spineart | Spineart | Other | Nationwide |
| Device | CLASS II | BioFlo DuraMax 15.5F Single Valve Sheath VascPak Kit recalled | Angiodynamics | Foreign Material | VA |
| Device | CLASS II | GE Healthcare Interact Discovery RT recalled by GE Medical Systems, SCS | GE Medical Systems SCS | Other | Nationwide |
| Device | CLASS II | Duraflow 2 Straight Basic Kit PG- Indicated for use recalled | Angiodynamics | Foreign Material | VA |
| Device | CLASS II | GE Healthcare Allia IGS recalled by GE Medical Systems, SCS | GE Medical Systems SCS | Other | Nationwide |
| Device | CLASS II | Duraflow 2 Straight Basic Kit -Indicated for use recalled | Angiodynamics | Foreign Material | VA |
| Device | CLASS II | Duramax Stacked Tip Str recalled by Angiodynamics | Angiodynamics | Foreign Material | VA |
| Device | CLASS II | Duramax Stacked Tip Str recalled by Angiodynamics | Angiodynamics | Foreign Material | VA |
| Device | CLASS I | GmbH, Vyaire Twin Tube sample line recalled by Vyaire Medical | Vyaire Medical | Other | Nationwide |
| Device | CLASS II | Intelli-C: Right side suspended Tabletop recalled by Nrt X-ray A/s | NRT X-ray | Device Malfunction | Nationwide |
| Device | CLASS I | BioZorb Marker-BioZorb 3D Bioabsorbable Marker recalled by Hologic | Hologic | Other | Nationwide |
| Device | CLASS II | Duramax Stacked Tip Str recalled by Angiodynamics | Angiodynamics | Foreign Material | VA |
| Device | CLASS III | Evidence MultiSTAT recalled by Randox Laboratories | Randox Laboratories | Packaging Defects | Nationwide |
| Device | CLASS II | Duraflow 2 Straight Basic Kit Pg-Indicated for use recalled | Angiodynamics | Foreign Material | VA |
| Drug | CLASS III | Sodium Sulfacetamide 10% - Sulfur 5% Cleanser recalledSodium Sulfacetamide 10 Sulfur 5 Cleanser | Acella Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Duloxetine Delayed-Release Capsules, USP, 20 mg recalledDuloxetine | Breckenridge Pharmaceutical | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Duloxetine Delayed-Release Capsules, USP, 30mg recalledDuloxetine | Breckenridge Pharmaceutical | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Duloxetine Delayed-Release Capsules, USP, 60 mg recalledDuloxetine | Breckenridge Pharmaceutical | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Clorazepate Dipotassium Tablets, USP, 3.75 mg, a) recalledClorazepate Dipotassium | Aurobindo Pharma USA | Other | Nationwide |
| Drug | CLASS II | traMADol Hydrochloride Tablets, USP 50 mg recalledTramadol Hydrochloride | Rubicon Research Private | Other | Nationwide |
| Drug | CLASS II | TraMADol HCl, Packaged as (a) recalled by RemedyRepack | RemedyRepack | Packaging Defects | Nationwide |
| Drug | CLASS II | Clorazepate Dipotassium Tablets, USP, 7.5 mg, a) recalledClorazepate Dipotassium | Aurobindo Pharma USA | Other | Nationwide |
| Drug | CLASS I | Javygtor (sapropterin dihydrochloride) Powder recalledJavygtor | Dr. Reddy's Laboratories | Potency & Assay | Nationwide |
| Drug | CLASS II | Amphotericin B Liposome for Injection, 50mg vials recalledAmphotericin B | SUN Pharmaceutical Industries | Potency & Assay | Nationwide |
| Drug | CLASS II | Timolol Maleate Ophthalmic Solution recalled by FDCTimolol Maleate | FDC | Packaging Defects | NJ |
| Drug | CLASS I | Sapropterin Dihydrochloride Powder for Oral Solution 100mg recalled | Dr. Reddy's Laboratories | Potency & Assay | Nationwide |
| Food | CLASS I | D-lo's Delightful Gourmet Cheesecake, Pistachio single serve recalledD-lo's Delightful | D-lo's Gourmet Cheesecake | Undeclared Wheat & Gluten | MI |
| Food | CLASS I | Homemade Ice Cream Horchata Gelato recalled by Belgian YummiesBelgian Yummies | Belgian Yummies | Undeclared Allergens | FL |
| Food | CLASS II | Tea Wafer - Vanilla Almond [Two sizes: of 8 wafers recalled | Sacramento Cookie Factory | Undeclared Allergens | 14 states |
| Food | CLASS III | Kirkman brand 5-MTHF Methyltetrahydrofolate 1mg capsule recalledKirkman | HTO Nevada | Labeling Errors | 6 states |
| Food | CLASS I | Salted Caramel Ice Cream Cookie Sandwich recalled by Belgian Yummies | Belgian Yummies | Undeclared Allergens | FL |
| Food | CLASS II | DB Yummers Sweet & Smokey Barbeque Sauce recalledDB Yummers | Detty Family Barbeque | Foreign Material | KY, OH |
| Food | CLASS II | Homemade Ice Cream Strawberry Gelato recalled by Belgian YummiesBelgian Yummies | Belgian Yummies | Undeclared Allergens | FL |
| Food | CLASS II | Homemade Ice Cream Birthday Cake Gelato recalled by Belgian YummiesBelgian Yummies | Belgian Yummies | Undeclared Allergens | FL |
| Food | CLASS II | DB Yummers Mildly Spicy Barbeque Sauce recalled by Detty Family BarbequeDB Yummers | Detty Family Barbeque | Foreign Material | KY, OH |
| Food | CLASS II | Original Wine Wafer - Lemon Vanilla [Two sizes recalled | Sacramento Cookie Factory | Undeclared Allergens | 14 states |
| Food | CLASS II | Java Wafer - Mocha Hazelnut [Two sizes: of 8 wafers recalledJava Wafer | Sacramento Cookie Factory | Undeclared Allergens | 14 states |
| Food | CLASS II | Goya Red Kidney Beans recalled by Tradewind Foods de Puerto RicoGoya | Tradewind Foods de Puerto Rico | Packaging Defects | PR |
| Food | CLASS I | Chocolate Ice Cream Cookie Sandwich recalled by Belgian Yummies | Belgian Yummies | Undeclared Allergens | FL |
| Food | CLASS I | Raspberry Ice Cream Cookie Sandwich recalled by Belgian Yummies | Belgian Yummies | Undeclared Allergens | FL |
| Food | CLASS II | Martinelli's Gold Medal Apple Juice From U.S. Grown Fresh recalledMartinelli's Gold | S Martinelli & | Lead & Heavy Metals | 35 states |
| Food | CLASS II | DB Yummers Island Marinade Barbeque Sauce recalledDB Yummers | Detty Family Barbeque | Foreign Material | KY, OH |
| Food | CLASS I | Key Lime Ice Cream Cookie Sandwich recalled by Belgian YummiesKey | Belgian Yummies | Undeclared Allergens | FL |
| Food | CLASS II | Champagne Wafer - Raspberry Almond [Two sizes recalledChampagne Wafer | Sacramento Cookie Factory | Undeclared Allergens | 14 states |
| Food | CLASS I | Peanut Butter Ice Cream Cookie Sandwich recalled by Belgian Yummies | Belgian Yummies | Undeclared Allergens | FL |
| Food | CLASS II | California Wine Wafer - Mocha Chocolate recalledCalifornia | Sacramento Cookie Factory | Undeclared Allergens | 14 states |
| Food | CLASS I | Vanilla Ice Cream Cookie Sandwich recalled by Belgian Yummies | Belgian Yummies | Undeclared Allergens | FL |
| Device | CLASS II | ZPLP (Zimmer Periarticular Locking Plate System) Distal recalled | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | ZPLP (Zimmer Periarticular Locking Plate System) Distal recalled | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | ZPLP (Zimmer Periarticular Locking Plate System) Distal recalled | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | Powerseal, Curved Jaw Sealer and Divider recalled | Olympus Corporation of the Americas | Packaging Defects | Nationwide |
| Device | CLASS I | HeartMate 3, LVAS Implant Kit recalled by Thoratec | Thoratec | Packaging Defects | Nationwide |
| Device | CLASS II | Powerseal, Curved Jaw Sealer and Divider recalled | Olympus Corporation of the Americas | Packaging Defects | Nationwide |
| Device | CLASS II | RayStation recalled by Raysearch Laboratories Ab | Raysearch Laboratories AB | Other | Nationwide |
| Device | CLASS II | RayStation 14.0.0.3338. Radiation Therapy Treatment Planning System recalled | Raysearch Laboratories AB | Other | Nationwide |
| Device | CLASS II | IPS e.max ZirCAD CER/in recalled by Ivoclar Vivadent Ag | Ivoclar Vivadent | Device Malfunction | Nationwide |
| Device | CLASS II | Sofsilk Braided Silk sutures, Product Number S-2782K recalled | Covidien | Sterility | CT |
| Device | CLASS II | ZPLP Distal Lateral Fibular Plate, Right, 10 Holes recalled by Zimmer | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | ZPLP Distal Lateral Fibular Plate, Left, 8 Holes recalled by Zimmer | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | IPS e.max ZirCAD CER/in recalled by Ivoclar Vivadent Ag | Ivoclar Vivadent | Device Malfunction | Nationwide |
| Device | CLASS II | ZPLP Distal Lateral Fibular Plate, Left, 4 Holes recalled by Zimmer | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | RayStation recalled by Raysearch Laboratories Ab | Raysearch Laboratories AB | Other | Nationwide |
| Device | CLASS II | Intellis AdaptiveStim Product Number 97715, Spinal Cord Stimulator recalled | Medtronic Neuromodulation | Other | MN |
| Device | CLASS II | ZPLP Distal Lateral Fibular Plate, Left, 10 Holes recalled by Zimmer | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | IPS e.max ZirCAD CER/in recalled by Ivoclar Vivadent Ag | Ivoclar Vivadent | Device Malfunction | Nationwide |
| Device | CLASS II | Lumbar Interbody Fusion System (Ollif) recalled | Advanced Research Medical | Other | Nationwide |
| Device | CLASS II | RayStation recalled by Raysearch Laboratories Ab | Raysearch Laboratories AB | Other | Nationwide |
| Device | CLASS II | Jackson-Pratt 3-Spring Reservoir Kit with PVC Round Drain recalled | Cardinal Health 200 | Sterility | Nationwide |
| Device | CLASS II | ZPLP(Zimmer Periarticular Locking Plate System) Distal recalled | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | ZPLP (Zimmer Periarticular Locking Plate System) Distal recalled | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | ZPLP (Zimmer Periarticular Locking Plate System) Distal recalled | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | RayStation 10.0.0.1154, 10.0.1.52 & 10.0.2.10. Radiation Therapy recalled | Raysearch Laboratories AB | Other | Nationwide |
| Device | CLASS II | IPS e.max ZirCAD CER/in recalled by Ivoclar Vivadent Ag | Ivoclar Vivadent | Device Malfunction | Nationwide |
| Device | CLASS II | Medtronic Invos, Reusable Sensor Cable for PM7100 recalled by Covidien | Covidien | Device Malfunction | 22 states |
| Device | CLASS II | Powerseal, Curved Jaw Sealer and Divider recalled | Olympus Corporation of the Americas | Packaging Defects | Nationwide |
| Device | CLASS II | RayStation 7.0.0.19. Radiation Therapy Treatment Planning System recalled | Raysearch Laboratories AB | Other | Nationwide |
| Device | CLASS II | ZPLP Distal Lateral Fibular Plate, Left, 4 Holes recalled by Zimmer | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | Keller Funnel recalled by Allergan Sales | Allergan Sales | Other | Nationwide |
| Device | CLASS II | Battery Mobile X-ray Unit Easy Moving recalled by Sedecal | Sedecal | Device Malfunction | Nationwide |
| Device | CLASS II | ZPLP (Zimmer Periarticular Locking Plate System) Distal recalled | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | The Distal Access Catheter is a single-lumen, braided shaft recalled | Stryker Neurovascular | Other | Nationwide |
| Device | CLASS II | RayStation 15.0.0.430. Radiation Therapy Treatment Planning System recalled | Raysearch Laboratories AB | Other | Nationwide |
| Device | CLASS II | ZPLP (Zimmer Periarticular Locking Plate System) Distal recalled | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | ZPLP (Zimmer Periarticular Locking Plate System) Distal recalled | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | ZPLP Distal Lateral Fibular Plate, Left, 6 Holes recalled by Zimmer | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | The Oncology Essentials Package of the Spectral CT imaging system recalled | Philips North America | Packaging Defects | Nationwide |
| Device | CLASS II | OsmoPRO MAX Automated Osmometer- IVD Osmometer for Clinical Use recalled | Advanced Instruments | Device Malfunction | Nationwide |
| Device | CLASS II | IPS e.max ZirCAD CER/in recalled by Ivoclar Vivadent Ag | Ivoclar Vivadent | Device Malfunction | Nationwide |
| Device | CLASS II | Jackson-Pratt 3-Spring Reservoir with Silicone Adapters recalled | Cardinal Health 200 | Sterility | Nationwide |
| Device | CLASS II | RayStation 8.0.0.61, 8.0.1.10. Radiation Therapy Treatment Planning recalled | Raysearch Laboratories AB | Other | Nationwide |
| Device | CLASS II | ZPLP Distal Lateral Fibular Plate, Right, 8 Holes recalled by Zimmer | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | ZPLP (Zimmer Periarticular Locking Plate System) Distal recalled | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | RayStation 11.0.0.951, 11.0.1.29, 11.0.3.116 & 11.0.4.15. Radiation recalled | Raysearch Laboratories AB | Other | Nationwide |
| Device | CLASS II | ZPLP Distal Lateral Fibular Plate, Left, 14 Holes recalled by Zimmer | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | ZPLP (Zimmer Periarticular Locking Plate System) Distal recalled | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | ZPLP Distal Lateral Fibular Plate, Right, 6 Holes recalled by Zimmer | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | Galaxy System recalled by Noah Medical | Noah Medical | Other | Nationwide |
| Device | CLASS II | Jackson-Pratt 3-Spring Reservoir Kit with PVC Round Drain recalled | Cardinal Health 200 | Sterility | Nationwide |
| Device | CLASS II | RayStation recalled by Raysearch Laboratories Ab | Raysearch Laboratories AB | Other | Nationwide |
| Device | CLASS II | ZPLP(Zimmer Periarticular Locking Plate System) Distal recalled | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | Jackson-Pratt Universal Connector PVC Tubing Anti Reflux recalled | Cardinal Health 200 | Sterility | Nationwide |
| Device | CLASS II | IPS e.max ZirCAD CER/in recalled by Ivoclar Vivadent Ag | Ivoclar Vivadent | Device Malfunction | Nationwide |
| Device | CLASS II | Cup Removal Starter Instrument recalled by Innomed | Innomed | Other | 11 states |
| Device | CLASS II | RayStation 8.1.0.47 recalled by Raysearch Laboratories Ab | Raysearch Laboratories AB | Other | Nationwide |
| Device | CLASS I | HeartMate 3, LVAS Implant Kit recalled by Thoratec | Thoratec | Packaging Defects | Nationwide |
| Device | CLASS II | Johnson & Johnson Vision Reusable Laminar High Flow recalled | Johnson & Johnson Surgical Vision | Other | Nationwide |
| Device | CLASS II | RayStation 13.0.0.1547, 13.1.0.144 & 13.1.1.89. Radiation Therapy recalled | Raysearch Laboratories AB | Other | Nationwide |
| Device | CLASS II | Jackson-Pratt 3-Spring Reservoir Kit with PVC Round Drain recalled | Cardinal Health 200 | Sterility | Nationwide |
| Device | CLASS II | Abbott Cholestech LDX Battery Kit recalled by Alere San Diego | Alere San Diego | E. coli | Nationwide |
| Device | CLASS II | Medtronic Invos, Reusable Infant Sensor Adapter Cable for PM7100 recalled | Covidien | Device Malfunction | 22 states |
| Drug | CLASS II | Eylea, (aflibercept) Injection, 2 mg of a 40mg/mL solution) recalledEylea | Regeneron Pharmaceuticals | Sterility | Nationwide |
| Drug | CLASS III | Valacyclovir Tablets USP, 500 mg recalled by ViatrisValacyclovir Hydrochloride | Viatris | Other | Nationwide |
| Drug | CLASS II | Methylergonovine Maleate Tablets, USP, 0.2mg recalledMethylergonovine Maleate | Amneal Pharmaceuticals of New York | Potency & Assay | Nationwide |
| Drug | CLASS III | Fentanyl 1000mcg/ (10mcg/mL) in 0.9% Sodium Chloride Injection recalled | Hikma Injectables USA | Packaging Defects | Nationwide |
| Drug | CLASS III | Epinephrine-Lidocaine HCl 0.25 mg/mL recalled by Imprimis NJOF | Imprimis Njof | Potency & Assay | Nationwide |
| Drug | CLASS II | Prednisolone Sodium Phosphate-Moxifloxacin-Bromfenac recalled | Imprimis Njof | Potency & Assay | Nationwide |
| Food | CLASS II | Longreen Corporation 4 in1 Cordyceps Coffee, 10 sachets/box recalledLongreen Corporation | BF Suma Pharmaceuticals | Undeclared Allergens | CA, TX |
| Food | CLASS I | King Kullen Broccoli Cutlets with Breadcrumbs and Parmesan recalledKing Kullen | Gracie's Kitchens | Undeclared Wheat & Gluten | NY |
| Food | CLASS II | French S Crispy Fried Onions Orig Pdm recalled | McCormick & Company, Inc.- Consumer Product Division | Other Bacterial Contamination | AZ, IL |
| Food | CLASS II | International Bread Pita Chips Retail Clamshell Container:, Bulk bag recalledInternational | International Pita Bread | Other | CA |
| Food | CLASS II | Bottle is labeled as Johnny's Parmesan Garlic Seasoning recalledBottle | OS Holding | Undeclared Sesame | 9 states |
| Food | CLASS II | Bizcocho de Boda Puertorrique¿o Naked "Puerto Rican recalledBizcocho | Reposteria Artesanal Laura | Mold | PR |
| Food | CLASS II | International Bread Pita Chips Retail Clamshell Container recalledInternational | International Pita Bread | Other | CA |
| Food | CLASS II | Longreen Corporation 4 in1 Reishi Coffee, 10 sachets/box recalledLongreen Corporation | BF Suma Pharmaceuticals | Undeclared Allergens | CA, TX |
| Food | CLASS II | French S Crispy Fried Onions Orig, Case Pack recalled | McCormick & Company, Inc.- Consumer Product Division | Other Bacterial Contamination | AZ, IL |
| Food | CLASS II | Longreen Corporation Xlim Express Coffee, 10 sachets/box recalledLongreen Corporation | BF Suma Pharmaceuticals | Undeclared Allergens | CA, TX |
| Food | CLASS II | Food Club All Purpose Flour Best if Used by 03/08/2025 recalled | Shawnee Milling | Undeclared Milk | OK |
| Food | HEALTH ALERT | Raw Pork Chorizo Products recalled by San Antonio Packing | San Antonio Packing | Foreign Material | |
| Device | CLASS II | Palindrome Precision H Chronic Catheter Kit 14./Ch recalled by Covidien | Covidien | Device Malfunction | Nationwide |
| Device | CLASS II | Acuson Juniper Diagnostic Ultrasound System recalled | Siemens Medical Solutions USA | Device Malfunction | Nationwide |
| Device | CLASS II | InflammaDry MMP-9 Test recalled by Quidel | Quidel | Hidden Drug Ingredients | 38 states |
| Device | CLASS II | Brand Name: Cleaner Bottle Product Name recalled | Electro Medical Systems | Device Malfunction | Nationwide |
| Device | CLASS II | Biomet OrthoPak Non-invasive Bone Growth Stimulator recalled by EBI | EBI | Other | Nationwide |
| Device | CLASS II | Various Alcon Custom Paks Surgical Procedure Pack recalled | Alcon Research | Particulate Matter | Nationwide |
| Device | CLASS II | 20" Lead Wires, Replacement recalled by EBI | EBI | Other | Nationwide |
| Device | CLASS II | Tridentii Hemi CLUSTER54E- Indicated for use in primary recalled | Howmedica Osteonics | Other | Nationwide |
| Device | CLASS II | Tridentii Hemi CLUSTER44B- Indicated for use in primary recalled | Howmedica Osteonics | Other | Nationwide |
| Device | CLASS II | 3M Durapore Surgical Tape recalled by 3M Company - Health Care | 3M Company - Health Care Business | Labeling Errors | Nationwide |
| Device | CLASS II | Tridentii PSL CLUSTER50D- Indicated for use in primary recalled | Howmedica Osteonics | Other | Nationwide |
| Device | CLASS II | Philips Patient Information Center recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Redux Electrolyte Creme, Product recalled by Parker Laboratories | Parker Laboratories | Other | Nationwide |
| Device | CLASS II | InflammaDry MMP-9 Test recalled by Quidel | Quidel | Hidden Drug Ingredients | 38 states |
| Device | CLASS I | 070 Reperfusion System recalled by Route 92 Medical | Route 92 Medical | Other | 26 states |
| Device | CLASS II | Tridentii Hemi CLUSTER58F- Indicated for use in primary recalled | Howmedica Osteonics | Other | Nationwide |
| Device | CLASS II | Acuson Maple Diagnostic Ultrasound System recalled | Siemens Medical Solutions USA | Device Malfunction | Nationwide |
| Device | CLASS II | Tridentii Hemi CLUSTER52E-Indicated for use in primary recalled | Howmedica Osteonics | Other | Nationwide |
| Device | CLASS I | Full Length 070 Access System recalled by Route 92 Medical | Route 92 Medical | Other | 26 states |
| Device | CLASS I | Vitek 2 - AST Test kits (in vitro diagnostic test cards recalled | Biomerieux | Other | MO |
| Device | CLASS II | Biomet SpinalPak Non-invasive Spine Fusion Stimulator recalled by EBI | EBI | Other | Nationwide |
| Device | CLASS II | Alinity m System recalled by Abbott Molecular | Abbott Molecular | Other | Nationwide |
| Device | CLASS II | Tridentii Hemi CLUSTER50D- Indicated for use in primary recalled | Howmedica Osteonics | Other | Nationwide |
| Device | CLASS II | Leica HistoCore Pegasus (Processor, Tissue, Automated) recalled | Leica Biosystems Nussloch | Other | Nationwide |
| Device | CLASS II | Tridentii PSL CLUSTER64H- Indicated for use in primary recalled | Howmedica Osteonics | Other | Nationwide |
| Device | CLASS II | Mariner RDX MIS Polyaxial Head recalled by Seaspine Orthopedics | Seaspine Orthopedics | Other | 4 states |
| Device | CLASS II | Mariner RDX Polyaxial Head recalled by Seaspine Orthopedics | Seaspine Orthopedics | Other | Nationwide |
| Device | CLASS II | LightStrike Blackout Curtains, Part numbers recalled | Xenex Disinfection Services | Other | Nationwide |
| Device | CLASS II | Palindrome Precision HSI Chronic Catheter Sport Pack 14./Ch recalled | Covidien | Device Malfunction | Nationwide |
| Device | CLASS I | Full Length 070 Reperfusion System recalled by Route 92 Medical | Route 92 Medical | Other | 26 states |
| Device | CLASS II | NexGen CR-Flex Femoral Component, Size E and Size E Minus (E-) recalled | Zimmer | Foreign Material | Nationwide |
| Device | CLASS II | 48" Lead Wires, Replacement recalled by EBI | EBI | Other | Nationwide |
| Device | CLASS II | Iba Proton Therapy System - Proteus 235, Pts-10 versions recalled | Ion Beam Applications | Other | Nationwide |
| Device | CLASS II | Tridentii PSL CLUSTER52E- Indicated for use in primary recalled | Howmedica Osteonics | Other | Nationwide |
| Device | CLASS II | Tridentii Hemi CLUSTER48D-indicated for use in primary recalled | Howmedica Osteonics | Other | Nationwide |
| Device | CLASS II | Brand Name: Piezon Bottle Product Name: Piezon Bottle Model/Catalog recalled | Electro Medical Systems | Device Malfunction | Nationwide |
| Device | CLASS II | Acuson Redwood 1.0 Diagnostic Ultrasound System recalled | Siemens Medical Solutions USA | Foreign Material | Nationwide |
| Device | CLASS II | Brand Name: Water Bottle Product Name: Water Bottle Model/Catalog recalled | Electro Medical Systems | Device Malfunction | Nationwide |
| Device | CLASS II | Tridentii Hemi CLUSTER66H- Indicated for use in primary recalled | Howmedica Osteonics | Other | Nationwide |
| Device | CLASS II | Vanguard Knee System AS Tibial Bearing / DCM ArCom recalled by Biomet | Biomet | Packaging Defects | Nationwide |
| Device | CLASS II | Tridentii PSL CLUSTER48D- Indicated for use in primary recalled | Howmedica Osteonics | Other | Nationwide |
| Device | CLASS II | Tridentii PSL CLUSTER58F-Indicated for use in primary recalled | Howmedica Osteonics | Other | Nationwide |
| Device | CLASS II | Baxter Seprafilm Adhesion Barrier 1 Half Sheet recalled | Baxter Healthcare | Other | Nationwide |
| Device | CLASS I | Tenzing 7 Delivery Catheter recalled by Route 92 Medical | Route 92 Medical | Other | 26 states |
| Device | CLASS I | 070 Access System recalled by Route 92 Medical | Route 92 Medical | Other | 26 states |
| Drug | CLASS I | GoHARD 25000, Male Sexual Enhancement, Honey, 100% Natural recalled | Pyramids Wholesale | Labeling Errors | Nationwide |
| Drug | CLASS II | minolira (minocycline hydrochloride) extended-release tablets, 105mg recalled | EPI Health | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS III | Abilify (aripiprazole) recalled by Second Tokushima FactoryAbilify | Second Tokushima Factory Otsuka Pharmaceutical | Packaging Defects | Nationwide |
| Drug | CLASS I | libigrow RED Dragon+, Maximum Strength Formula recalled | Pyramids Wholesale | Labeling Errors | Nationwide |
| Drug | CLASS II | Diltiazem Hydrochloride Extended-Release Capsules recalledDiltiazem Hydrochloride | Glenmark Pharmaceuticals Inc., USA | Potency & Assay | Nationwide |
| Drug | CLASS II | Ful-glo, Fluorescein Sodium Sterile Ophthalmic Strips recalled by Nomax | Nomax | Potency & Assay | Nationwide |
| Drug | CLASS II | Cloderm (clocortolone pivalate) Cream recalled by EPI Health | EPI Health | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | GloStrips, Fluorescein Sodium Ophthalmic Strips recalled by NomaxGlostrips | Nomax | Potency & Assay | Nationwide |
| Drug | CLASS II | Eyesaline, Saline Eyewash Solution, Cartridge recalled by HoneywellFendall 2000 Pure Flow | Honeywell | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS I | The Goat Sublingual Strip, Male Enhancement recalled | Pyramids Wholesale | Labeling Errors | Nationwide |
| Drug | CLASS I | Silverback Xxx Power Male Enhancement recalled by Pyramids Wholesale | Pyramids Wholesale | Labeling Errors | Nationwide |
| Drug | CLASS I | Honey Manuka Bunny Love, All Natural Sexual Enhancement recalled | Pyramids Wholesale | Labeling Errors | Nationwide |
| Drug | CLASS I | Alphastrip Male Performance Enhancer recalled by Pyramids Wholesale | Pyramids Wholesale | Labeling Errors | Nationwide |
| Drug | CLASS III | Abilify (aripiprazole) recalled by Second Tokushima FactoryAbilify | Second Tokushima Factory Otsuka Pharmaceutical | Packaging Defects | Nationwide |
| Drug | CLASS II | minolira (minocycline hydrochloride) extended-release tablets, 135mg recalled | EPI Health | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS III | Abilify (aripiprazole) recalled by Second Tokushima FactoryAbilify | Second Tokushima Factory Otsuka Pharmaceutical | Packaging Defects | Nationwide |
| Drug | CLASS II | Ipratropium Bromide and Albuterol Sulfate Inhalation recalledIpratropium Bromide And Albuterol Sulfate | Cipla USA | Packaging Defects | Nationwide |
| Drug | CLASS I | Samurai-X Honey recalled by Pyramids Wholesale | Pyramids Wholesale | Labeling Errors | Nationwide |
| Drug | CLASS I | Spanish Fly 22K capsules recalled by Pyramids Wholesale | Pyramids Wholesale | Labeling Errors | Nationwide |
| Drug | CLASS III | Abilify (aripiprazole) recalled by Second Tokushima FactoryAbilify | Second Tokushima Factory Otsuka Pharmaceutical | Packaging Defects | Nationwide |
| Drug | CLASS I | Pink Pussycat Honey recalled by Pyramids Wholesale | Pyramids Wholesale | Labeling Errors | Nationwide |
| Drug | CLASS II | Ful-glo, Fluorescein Sodium Ophthalmic Strips USP 1 mg recalled by Nomax | Nomax | Potency & Assay | Nationwide |
| Drug | CLASS II | GloStrips, Fluorescein Sodium Ophthalmic Strips recalled by NomaxGlostrips | Nomax | Potency & Assay | Nationwide |
| Drug | CLASS I | Aruba Aloe Hand Sanitizer Gel, 80% Alcohol recalled | Aruba Aloe Balm N.V | Foreign Material | Nationwide |
| Drug | CLASS I | ForeverMen Natural Energy Boost Capsules recalled by FA Online | FA Online | Labeling Errors | Nationwide |
| Drug | CLASS I | Flower Power, CBD infused Female Enhancement recalled | Pyramids Wholesale | Labeling Errors | Nationwide |
| Drug | CLASS I | Alcoholada Gel, Pain Relieving Gel, 0.5% Lidocaine Hydrochloride recalled | Aruba Aloe Balm N.V | Foreign Material | Nationwide |
| Drug | CLASS I | Weiner Boner Honey packet, 100% Organic Formula recalled | Pyramids Wholesale | Labeling Errors | Nationwide |
| Food | CLASS I | Ground Beef Products recalled by Cargill Beef | Cargill Beef | E. coli | |
| Food | CLASS I | Roly Poly Bakery Multigrain bread recalledRoly Poly | Roly-Poly Bakery | Undeclared Egg | CT, MA |
| Food | CLASS III | Aluminum cans of root beer packaged recalled by PepsicoAluminum | Pepsico | Labeling Errors | 6 states |
| Food | CLASS II | Ready Meals Teriyaki Salmon W Rice Tray Blk&gold Alum recalled | Taylor Farms Southwest | Labeling Errors | AZ |
| Food | CLASS III | Blues Hog Sweet & Savory Seasoning recalled by Baron SpicesBlues Hog | Baron Spices | Undeclared Wheat & Gluten | MO |
| Food | CLASS II | Kowalski Simply Sides - Jack's Potato Salad recalled by Home Style FoodsKowalski Simply | Home Style Foods | Undeclared Egg | MI |
| Food | CLASS II | Enchilada Verde Whole Meal recalled by Amy's KitchenAmy's | Amy's Kitchen | Other | 21 states |