| Food | CLASS I | Sausage Link Products recalled by D. J.'s Boudain | D. J.'s Boudain | Foreign Material | |
| Device | CLASS II | Codman Certas Plus Programmable Valve Inline Small Valve Only recalled | Integra LifeSciences | Packaging Defects | Nationwide |
| Device | CLASS II | Otological Ventilation Tube - Donaldson - Double - Blue Silicone recalled | Adept Medical | Other | Nationwide |
| Device | CLASS II | Otological Ventilation Tube - T-Tube - Double - Silicone recalled | Adept Medical | Other | Nationwide |
| Device | CLASS II | Select Series Angled Tip Arterial Cannula recalled | Medtronic Perfusion Systems | Labeling Errors | Nationwide |
| Device | CLASS II | Codman Certas Plus Programmable Valve Right Angle Valve Only recalled | Integra LifeSciences | Packaging Defects | Nationwide |
| Device | CLASS II | N/A Repeater Bone Tamp recalled by Integrity Implants | Integrity Implants | Device Malfunction | Nationwide |
| Device | CLASS II | Cardiomems HF Pressure Measurement System CardioMEMSTM HF recalled | St. Jude Medical | Labeling Errors | Nationwide |
| Device | CLASS II | Thunderbeat ,Front-actuated Grip Type S recalled | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Cardiomems HF Pressure Measurement System CardioMEMSTM HF recalled | St. Jude Medical | Labeling Errors | Nationwide |
| Device | CLASS II | Tacy Medical, Inc Dressing Change Tray CS/20 recalled by Trinity Sterile | Trinity Sterile | Sterility | Nationwide |
| Device | CLASS II | Thunderbeat, Front-actuated Grip Type S¿ recalled | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Thunderbeat, Front-actuated Grip Type S recalled | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | BD Pyxis MedStation 4000 AUX recalled by CareFusion 303 | CareFusion 303 | Device Malfunction | CA |
| Device | CLASS II | EOPA Arterial Cannula recalled by Medtronic Perfusion Systems | Medtronic Perfusion Systems | Labeling Errors | Nationwide |
| Device | CLASS II | Otological Ventilation Tube - T-Tube - Silicone recalled | Adept Medical | Other | Nationwide |
| Device | CLASS II | Baxter Clearlink System Solution Set with Duo-Vent Spike recalled | Baxter Healthcare | Other | Nationwide |
| Device | CLASS II | Baxter Solution Set with Duo-Vent Spike recalled by Baxter Healthcare | Baxter Healthcare | Other | Nationwide |
| Device | CLASS II | Randox Lipoprotein (a) - In vitro diagnostic recalled | Randox Laboratories | Device Malfunction | Nationwide |
| Device | CLASS II | Codman Certas Plus Programmable Valve Inline Small Valve Only recalled | Integra LifeSciences | Packaging Defects | Nationwide |
| Device | CLASS II | BD Pyxis Med 4000 Auxiliary (AUX) recalled by CareFusion 303 | CareFusion 303 | Device Malfunction | CA |
| Device | CLASS II | Bodor P and C series laser cutting machines recalled | Jinan Bodor Cnc Machine | Other | Nationwide |
| Device | CLASS II | Otological Ventilation Tube - T-Tube - Silicone recalled | Adept Medical | Other | Nationwide |
| Device | CLASS II | Thunderbeat Front-Actuated Grip Type S recalled | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Thunderbeat,Front-actuated Grip Type S recalled | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Merlin.net Patient Care Network recalled by St. Jude Medical | St. Jude Medical | Device Malfunction | 13 states |
| Device | CLASS II | Randox Lipoprotein (a) - In vitro diagnostic recalled | Randox Laboratories | Device Malfunction | Nationwide |
| Device | CLASS II | Thunderbeat, Front-actuated Grip Type S recalled | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Vitros 3600 Immunodiagnostic System recalled | Ortho-Clinical Diagnostics | Device Malfunction | Nationwide |
| Device | CLASS II | Thunderbeat, Front-actuated Grip Type S recalled | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Otological Ventilation Tube - T-Tube - Double - Silicone recalled | Adept Medical | Other | Nationwide |
| Device | CLASS II | Vitros 5600 Integrated System recalled by Ortho-Clinical Diagnostics | Ortho-Clinical Diagnostics | Device Malfunction | Nationwide |
| Device | CLASS II | Vitros XT 7600 Integrated System recalled by Ortho-Clinical Diagnostics | Ortho-Clinical Diagnostics | Device Malfunction | Nationwide |
| Device | CLASS II | Wolf-Pak Dressing Change Kit recalled by Trinity Sterile | Trinity Sterile | Sterility | Nationwide |
| Device | CLASS II | Wolf-Pak Dressing Change Kit recalled by Trinity Sterile | Trinity Sterile | Sterility | Nationwide |
| Device | CLASS II | IMed Products Dressing Change Kit with ChloraPrep & HaloGUARD recalled | Trinity Sterile | Sterility | Nationwide |
| Device | CLASS II | Halyard Laparotomy Pack recalled by O&m Halyard | O&M Halyard | Sterility | Nationwide |
| Device | CLASS II | DLP Pediatric One-Piece Arterial Cannulae recalled | Medtronic Perfusion Systems | Labeling Errors | Nationwide |
| Device | CLASS II | BD PCR Cartridges used with MAX System recalled by Becton Dickinson & | Becton Dickinson | Other | Nationwide |
| Device | CLASS II | Headway" 17 Advanced Straight Microcatheter with Hydrophilic Coating recalled | Microvention | Sterility | CA |
| Device | CLASS II | The Neuro Match Head Soft Touch bur recalled by Stryker | Stryker | Packaging Defects | Nationwide |
| Device | CLASS II | Thunderbeat,Front-actuated Grip Type S recalled | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Baxter Continu-Flo Solution Set with Duo-Vent Spike recalled | Baxter Healthcare | Other | Nationwide |
| Device | CLASS II | Otological Ventilation Tube - Donaldson - Blue Silicone recalled | Adept Medical | Other | Nationwide |
| Device | CLASS II | Thunderbeat, Front-actuated Grip Type S recalled | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Precision Neuro Match Head recalled by Stryker | Stryker | Packaging Defects | Nationwide |
| Device | CLASS II | Thunderbeat,Front-actuated Grip Type S recalled | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Wolf-Pak Premium Dressing Change Kit with GuardiVa & Statlock CS/30 recalled | Trinity Sterile | Sterility | Nationwide |
| Device | CLASS II | Neuro Match Head recalled by Stryker | Stryker | Packaging Defects | Nationwide |
| Device | CLASS II | Otological Ventilation Tube - T-Tube - Double - Silicone recalled | Adept Medical | Other | Nationwide |
| Device | CLASS II | BD Pyxis Med ES Auxiliary (AUX) recalled by CareFusion 303 | CareFusion 303 | Device Malfunction | CA |
| Device | CLASS II | Thunderbeat, Front-actuated Grip Type S recalled | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS I | VDR4 Phasitron Breathing Circuit recalled by Percussionaire | Percussionaire | Other | Nationwide |
| Device | CLASS II | Otological Ventilation Tube - T-Tube - Silicone recalled | Adept Medical | Other | Nationwide |
| Drug | CLASS III | Venlafaxine Extended-Release Tablets, 150mg recalled by Appco PharmaVenlafaxine | Appco Pharma | Other | Nationwide |
| Drug | CLASS I | Fouzee SugarLin Herbal Formula capsules per, Sold recalled | Shoppers- Plaza | Labeling Errors | Nationwide |
| Drug | CLASS II | Ultra Repair Cream, colloidal oatmeal 0.5%, Coconut Vanilla recalled | First Aid Beauty | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Kissable Diabetics Foot Cream recalled by Brands International | Brands International | Manufacturing (CGMP) Deviations | Nationwide |
| Food | CLASS I | Marketside, Broccoli Florets, Best IF Used BY Dec recalledMarketside | Braga Fresh Foods | Listeria | 20 states |
| Food | CLASS I | Cal Yee's Dark Chocolate Almonds) recalled by Cal Yee FarmCal Yee's | Cal Yee Farm | Undeclared Milk | CA, PA |
| Food | CLASS III | & Kitchens Spinach Artichoke Dip Mix recalled by River Valley RanchRiver Valley | River Valley Ranch | Processing Deviation | WI |
| Food | CLASS I | Cal Yee's New Orleans Hot Mix) recalled by Cal Yee FarmCal Yee's | Cal Yee Farm | Undeclared Wheat & Gluten | CA, PA |
| Food | CLASS I | Cal Yee's Tropical Trail Mix - assorted nuts and dried fruits) recalledCal Yee's | Cal Yee Farm | Undeclared Milk | CA, PA |
| Food | CLASS II | Fruit Basket recalled by Cal Yee FarmCal Yee | Cal Yee Farm | Undeclared Tree Nuts | CA, PA |
| Food | CLASS I | Cal Yee's Cajun Sesame Hot Sticks) recalled by Cal Yee FarmCal Yee's | Cal Yee Farm | Undeclared Wheat & Gluten | CA, PA |
| Food | CLASS I | Kirkland Signature Smoked Salmon recalled by Acme Smoked FishKirkland Signature | Acme Smoked Fish | Listeria | FL |
| Food | CLASS II | Buttered Vegetables Keep Frozen recalled by Lidl US TRADINGButtered Vegetables | Lidl US TRADING | Undeclared Milk | 10 states |
| Food | CLASS I | Dark Chocolate Apricots) Cal Yee Farms Dark Chocolate Apricots) recalledCal Yee | Cal Yee Farm | Undeclared Milk | CA, PA |
| Food | CLASS I | Cal Yee's Dark Chocolate Raisins) recalled by Cal Yee FarmCal Yee's | Cal Yee Farm | Undeclared Milk | CA, PA |
| Food | CLASS I | Cal Yee's Dark Chocolate Walnuts) recalled by Cal Yee FarmCal Yee's | Cal Yee Farm | Undeclared Milk | CA, PA |
| Food | CLASS I | Cal Yee's Yogurt Coated Almonds recalled by Cal Yee FarmCal Yee's | Cal Yee Farm | Undeclared Milk | CA, PA |
| Food | CLASS II | Horizon Organic Aseptic Plain Whole Milk Refrigerate after opening recalledHorizon | Horizon Organic Dairy | Mold | AZ, CA, NV |
| Food | CLASS II | Mr. Bing brand Sriracha Chili Sauce recalledMr. Bing | Mr Bing Foods | Mold | 9 states |
| Food | CLASS II | The OG Bar;; Ingredients: Oats, brown sugar, honey, almonds recalled | The Granola Bar | Undeclared Milk | CT, NY |
| Food | CLASS II | Cal Yee's Butter Toffee Almonds) Boa Vista Butter Toffee Almonds) recalledCal Yee's | Cal Yee Farm | Undeclared Milk | CA, PA |
| Food | CLASS II | Cal Yee's Dried Mangos with Chili) recalled by Cal Yee FarmCal Yee's | Cal Yee Farm | Undeclared Allergens | CA, PA |
| Food | HEALTH ALERT | Wegmans Frozen Fully Cooked Chicken Nuggets recalled by Perdue Foods | Perdue Foods | Foreign Material | |
| Device | CLASS I | Welch Allyn, Inc., Life2000 Ventilation System recalled | Baxter Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Cardinal Health Presource Kits: 1 ) Triple Endo Pack recalled | Cardinal Health 200 | Sterility | Nationwide |
| Device | CLASS II | Idylla Instrument, IVD recalled by Biocartis Nv | Biocartis | Other | 5 states |
| Device | CLASS II | Fenestrated Bipolar Forceps,is4000 recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS II | GE Healthcare Varicam Millennium VG Discovery VH recalled | GE Medical Systems Israel Functional Imaging | Other | |
| Device | CLASS II | Monitoring System recalled by Murata Vios | Murata Vios | Device Malfunction | Nationwide |
| Device | CLASS II | Long Bipolar Grasper,is4000 recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS II | Karl Storz - Endoskope recalled | Karl Storz Endoscopy | Sterility | 32 states |
| Device | CLASS II | Vitros Chemistry Products Dgxn Slides recalled by Quidel Ortho | Quidel Ortho | Device Malfunction | Nationwide |
| Device | CLASS II | Econo Sterile medical procedure kits labeled as recalled | Sklar Instruments | Sterility | Nationwide |
| Device | CLASS II | Econo Sterile medical procedure kits labeled as recalled | Sklar Instruments | Sterility | Nationwide |
| Device | CLASS II | Mega Suturecut Nd,is4000¿ recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS II | LithoCrushV Single Use Mechanical Lithotriptor recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Tenaculum Forceps,is4000¿ recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS II | Cadiere Forceps,is4000 ¿ recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS II | Esteem Synergy Stomahesive Skin Barrier recalled by ConvaTec | ConvaTec | Packaging Defects | IL, NY, OH |
| Device | CLASS II | Dual Blade Retractor,is4000¿ recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS II | Tip-up Fenestrated Grasper,is4000¿ recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS I | Medline Fluid Delivery Set with Drip Chamber recalled | Medline Industries LP - Northfield | Other | Nationwide |
| Device | CLASS II | GE Healthcare Discovery NM/CT 670 PRO recalled | GE Medical Systems Israel Functional Imaging | Other | |
| Device | CLASS II | Small Grasping Retractor,is4000¿ recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS II | Cobra Grasper,is4000 recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS II | GE Healthcare Discovery NM recalled by Ge Medical Systems Israel | GE Medical Systems Israel Functional Imaging | Other | |
| Device | CLASS I | Altrua 2 DR Pacemaker, SL recalled by Boston Scientific | Boston Scientific | Device Malfunction | Nationwide |
| Device | CLASS II | Cardinal Health Presource Kits: 1 ) Kit, Major Oral Surgery recalled | Cardinal Health 200 | Sterility | Nationwide |
| Device | CLASS I | Impella RP with SmartAssist recalled by Abiomed | Abiomed | Device Malfunction | Nationwide |
| Device | CLASS II | Large Suturecut Needle Driver,is4000¿ recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS I | Welch Allyn, Inc., Life2000 Ventilation System recalled | Baxter Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Econo Sterile medical procedure kits labeled as recalled | Sklar Instruments | Sterility | Nationwide |
| Device | CLASS I | Sheath, 18 Fr., 160 mm (REF: WA2PS18L), gastroenterology-urology recalled | Trokamed | Other | PA |
| Device | CLASS II | Econo Sterile medical procedure kits labeled as recalled | Sklar Instruments | Sterility | Nationwide |
| Device | CLASS II | Econo Sterile medical procedure kits labeled as recalled | Sklar Instruments | Sterility | Nationwide |
| Device | CLASS II | Augustine Surgical Inc. Hot Dog Patient Warming recalled | Augustine Temperature Management | Temperature Abuse | MN |
| Device | CLASS II | Econo Sterile medical procedure kits labeled as recalled | Sklar Instruments | Sterility | Nationwide |
| Device | CLASS II | Cardinal Health Presource Kits: 1 ) Laryngoscopy Pack recalled | Cardinal Health 200 | Sterility | Nationwide |
| Device | CLASS II | Folysil Silicone Foley Catheters recalled by Coloplast Manufacturing US | Coloplast Manufacturing US | Sterility | Nationwide |
| Device | CLASS II | GE Healthcare Infinia II Hawkeye recalled by Ge Medical Systems Israel | GE Medical Systems Israel Functional Imaging | Other | |
| Device | CLASS I | Visionist Crt-p, El recalled by Boston Scientific | Boston Scientific | Device Malfunction | Nationwide |
| Device | CLASS II | GE Healthcare Optima NM/CT recalled by Ge Medical Systems Israel | GE Medical Systems Israel Functional Imaging | Other | |
| Device | CLASS II | Econo Sterile medical procedure kits labeled as recalled | Sklar Instruments | Sterility | Nationwide |
| Device | CLASS II | Micro Bipolar Forceps,is4000 ¿ recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS II | Medium-large Clip Applier,is4000¿ recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS II | Potts Scissors, Is4000 recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS II | Econo Sterile medical procedure kits labeled as recalled | Sklar Instruments | Sterility | Nationwide |
| Device | CLASS II | Large Hem-o-lok Clip Applier,is4000¿ recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS II | Curved Bipolar Dissector,is4000¿ recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS II | Stryker Blueprint Mixed Reality BP MxR Glenoid Pin Guide recalled | Tornier S.A.S | Foreign Material | 7 states |
| Device | CLASS II | Force Bipolar,is4000 recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS II | Round Tip Scissors, Is4000 ¿ recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS II | Econo Sterile medical procedure kits labeled as recalled | Sklar Instruments | Sterility | Nationwide |
| Device | CLASS II | Econo Sterile medical procedure kits labeled as recalled | Sklar Instruments | Sterility | Nationwide |
| Device | CLASS II | Micro Bipolar Forceps,is4000 recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS II | GE Healthcare Infinia II recalled by Ge Medical Systems Israel | GE Medical Systems Israel Functional Imaging | Other | |
| Device | CLASS II | GE Healthcare Infinia I Hawkeye recalled by Ge Medical Systems Israel | GE Medical Systems Israel Functional Imaging | Other | |
| Device | CLASS II | Change Healthcare Cardiology Hemodynamics recalled by A L I Technologies | A L I Technologies | Device Malfunction | Nationwide |
| Device | CLASS II | Econo Sterile medical procedure kits labeled as recalled | Sklar Instruments | Sterility | Nationwide |
| Device | CLASS II | Curved Bipolar Dissector,is4000 recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS I | Neo-Tee T-Piece Resuscitator recalled by Mercury Enterprises | Mercury Enterprises | Other | Nationwide |
| Device | CLASS II | Large Suturecut Needle Driver,is4000 recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS II | Augustine Surgical Inc. Hot Dog Patient Warming recalled | Augustine Temperature Management | Temperature Abuse | MN |
| Device | CLASS I | Sheath, 20 Fr., 130 mm (REF: WA2PS20S), gastroenterology-urology recalled | Trokamed | Other | PA |
| Device | CLASS II | Econo Sterile medical procedure kits labeled as recalled | Sklar Instruments | Sterility | Nationwide |
| Device | CLASS II | Tenaculum Forceps recalled by Intuitive Surgical | Intuitive Surgical | Device Malfunction | Nationwide |
| Device | CLASS II | Force Bipolar,is4000 recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS II | OsteoCove Putty, 1.25cc recalled by IsoTis OrthoBiologics | IsoTis OrthoBiologics | Other | Nationwide |
| Device | CLASS II | Small Graptor recalled by Intuitive Surgical | Intuitive Surgical | Device Malfunction | Nationwide |
| Device | CLASS II | BD Pyxis MedStation ES (Med ES Main) recalled by CareFusion 303 | CareFusion 303 | Device Malfunction | Nationwide |
| Device | CLASS II | Medical procedure kits labeled as recalled by Sklar Instruments | Sklar Instruments | Sterility | Nationwide |
| Device | CLASS II | Cook Medical Biodesign Dural Graft recalled by Cook Biotech | Cook Biotech | Other | MI |
| Device | CLASS II | Cook Medical Biodesign Otologic Butterfly Graft recalled by Cook Biotech | Cook Biotech | Other | MI |
| Device | CLASS II | Vitros Chemistry Products Dgxn Slides recalled by Quidel Ortho | Quidel Ortho | Device Malfunction | Nationwide |
| Device | CLASS II | Medtronic NanoCross Elite PTA catheter recalled by ev3 | ev3 | Other | Nationwide |
| Device | CLASS II | Econo Sterile medical procedure kits labeled as recalled | Sklar Instruments | Sterility | Nationwide |
| Device | CLASS II | Econo Sterile medical procedure kits labeled as recalled | Sklar Instruments | Sterility | Nationwide |
| Device | CLASS I | Breathe Technologies, Inc., Life2000 Ventilation System recalled | Baxter Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Maryland Bipolar Forceps,is4000 recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS II | Debakey Forceps,is4000 ¿ recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS II | Maryland Bipolar Forceps,is4000 ¿ recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS II | Prograsp Forceps,is4000 ¿ recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS II | Cadiere Forceps,is4000 recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS II | Econo Sterile medical procedure kits labeled as recalled | Sklar Instruments | Sterility | Nationwide |
| Device | CLASS II | DRG:HYBRiD-XL Insulin recalled by DRG International | DRG International | Potency & Assay | Nationwide |
| Device | CLASS II | Econo Sterile medical procedure kits labeled as recalled | Sklar Instruments | Sterility | Nationwide |
| Device | CLASS II | Hillrom Temperature Management Controller, MP recalled | Augustine Temperature Management | Temperature Abuse | MN |
| Device | CLASS II | OsteoSurge 100 Demineralized Bone Matrix Putty recalled | IsoTis OrthoBiologics | Device Malfunction | Nationwide |
| Device | CLASS II | McKesson Cardiology Hemo recalled by A L I Technologies | A L I Technologies | Device Malfunction | Nationwide |
| Device | CLASS II | Econo Sterile medical procedure kits labeled as recalled | Sklar Instruments | Sterility | Nationwide |
| Device | CLASS II | Mega Needle Driver,is4000¿ recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS II | Econo Sterile medical procedure kits labeled as recalled | Sklar Instruments | Sterility | Nationwide |
| Device | CLASS II | GE Healthcare Discovery NM/CT recalled by Ge Medical Systems Israel | GE Medical Systems Israel Functional Imaging | Other | |
| Device | CLASS II | VerifyNow P2Y12 Platelet Reactivity Test recalled by Accriva Diagnostics | Accriva Diagnostics | Other | Nationwide |
| Device | CLASS II | Portrait Core Services, a set recalled by GE Medical Systems | GE Medical Systems | Device Malfunction | Nationwide |
| Device | CLASS II | Econo Sterile medical procedure kits labeled as recalled | Sklar Instruments | Sterility | Nationwide |
| Device | CLASS I | Valitude Crt-p, El recalled by Boston Scientific | Boston Scientific | Device Malfunction | Nationwide |
| Device | CLASS II | GE Healthcare Discovery NM/CT 670 ES recalled | GE Medical Systems Israel Functional Imaging | Other | |
| Device | CLASS II | Behavioral Health Hospital bed side rails recalled | NOA Medical Industries | Device Malfunction | 4 states |
| Device | CLASS I | Sheath, 20 Fr., 160 mm (REF: WA2PS20L), gastroenterology-urology recalled | Trokamed | Other | PA |
| Device | CLASS II | Econo Sterile medical procedure kits labeled as recalled | Sklar Instruments | Sterility | Nationwide |
| Device | CLASS II | Cardinal Health Presource Kits: 1 ) Kit, Fetal Surgery recalled | Cardinal Health 200 | Sterility | Nationwide |
| Device | CLASS II | Econo Sterile medical procedure kits labeled as recalled | Sklar Instruments | Sterility | Nationwide |
| Device | CLASS II | Change Healthcare Cardiology Hemo recalled by A L I Technologies | A L I Technologies | Device Malfunction | Nationwide |
| Device | CLASS II | GE Healthcare Discovery NM/CT 670 DR recalled | GE Medical Systems Israel Functional Imaging | Other | |
| Device | CLASS II | Econo Sterile medical procedure kits labeled as recalled | Sklar Instruments | Sterility | Nationwide |
| Device | CLASS II | Econo Sterile medical procedure kits labeled as recalled | Sklar Instruments | Sterility | Nationwide |
| Device | CLASS II | Resano Forceps,is4000 ¿ recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS II | GE Healthcare Discovery NM/CT 670 CZT recalled | GE Medical Systems Israel Functional Imaging | Other | |
| Device | CLASS II | Cardinal Health Presource Kits: Kit, H N Free Flap recalled | Cardinal Health 200 | Sterility | Nationwide |
| Device | CLASS II | GE Healthcare Infinia recalled by Ge Medical Systems Israel | GE Medical Systems Israel Functional Imaging | Other | |
| Device | CLASS II | Econo Sterile medical procedure kits labeled as recalled | Sklar Instruments | Sterility | Nationwide |
| Device | CLASS II | GE Healthcare Brivo NM recalled by Ge Medical Systems Israel | GE Medical Systems Israel Functional Imaging | Other | |
| Device | CLASS II | Alcon Monarch¿ III D Delivery Cartridge recalled by Alcon Research | Alcon Research | Device Malfunction | 42 states |
| Device | CLASS II | Black Diamond Micro Forceps,is4000 ¿ recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS II | Econo Sterile medical procedure kits labeled as recalled | Sklar Instruments | Sterility | Nationwide |
| Device | CLASS II | Cardinal Health Presource Kits: 1 ) Aneurysm Pack recalled | Cardinal Health 200 | Sterility | Nationwide |
| Device | CLASS I | AquaFlexFlow UF 500 Plus recalled by Nuwellis | Nuwellis | Device Malfunction | Nationwide |
| Device | CLASS II | Long Tip Forceps,is4000 recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS I | Impella RP Flex with SmartAssist recalled by Abiomed | Abiomed | Device Malfunction | Nationwide |
| Device | CLASS II | Fenestrated Bipolar Forceps,is4000¿ recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS I | Medline Fluid Delivery Set with Drip Chamber recalled | Medline Industries LP - Northfield | Other | Nationwide |
| Device | CLASS II | Atrial Retractor Short Right,is4000¿ recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS II | Econo Sterile medical procedure kits labeled as recalled | Sklar Instruments | Sterility | Nationwide |
| Device | CLASS I | Sheath, 18 Fr., 130 mm (REF: WA2PS18S), gastroenterology-urology recalled | Trokamed | Other | PA |
| Device | CLASS II | Monopolar Curved Scissors, Is4000 recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS II | Econo Sterile medical procedure kits labeled as recalled | Sklar Instruments | Sterility | Nationwide |
| Device | CLASS II | Implant Epikut S Plus CM 16-Degrees recalled by Sin Sistema De Implante | SIN Sistema De Implante Nacional | Labeling Errors | 10 states |
| Device | CLASS II | Augustine Surgical Inc. Hot Dog Patient Warming recalled | Augustine Temperature Management | Temperature Abuse | MN |
| Device | CLASS II | Panther Fusion GBS Assay recalled by Hologic | Hologic | Potency & Assay | 20 states |
| Device | CLASS II | Cook Medical Biodesign Hiatal Hernia Graft recalled by Cook Biotech | Cook Biotech | Other | MI |
| Device | CLASS I | Olympus MAJ-891 Forceps/Irrigation Plug (Isolated Type) recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Econo Sterile medical procedure kits labeled as recalled | Sklar Instruments | Sterility | Nationwide |
| Device | CLASS II | Prograsp Forceps,is4000 recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS II | Large Needle Driver, Is4000 recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS II | Econo Sterile medical procedure kits labeled as recalled | Sklar Instruments | Sterility | Nationwide |
| Device | CLASS II | Mega Suturecut Nd,is4000 recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS II | X-Flow prostatectomy catheter recalled by Coloplast Manufacturing US | Coloplast Manufacturing US | Sterility | Nationwide |
| Device | CLASS II | Horizon Small Clip Applier,is4000¿ recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS II | Augustine Surgical Inc. Hot Dog Patient Warming recalled | Augustine Temperature Management | Temperature Abuse | MN |
| Device | CLASS I | Welch Allyn, Inc., Life 2000 Ventilation System recalled | Baxter Healthcare | Device Malfunction | Nationwide |
| Drug | CLASS III | Acetaminophen Extra Strength 500 mg per, Akron Pharma recalled | Akron Pharma | Other | Nationwide |
| Drug | CLASS II | Cardura XL (doxazosin) extended release tablets 4 mg recalled by ViatrisCardura | Viatris | Potency & Assay | Nationwide |
| Drug | CLASS III | Acetaminophen Extra Strength 500 mg per, Akron Pharma, Inc. recalled | Akron Pharma | Other | Nationwide |
| Drug | CLASS III | Diphenhydramine HCl 25 mg per, Akron Pharma recalled | Akron Pharma | Other | Nationwide |
| Drug | CLASS II | Cardura XL (doxazosin) extended release tablets 8 mg recalled by ViatrisCardura | Viatris | Potency & Assay | Nationwide |
| Drug | CLASS III | Acetaminophen Regular Strength, 325 mg per, Akron Pharma recalled | Akron Pharma | Other | Nationwide |
| Drug | CLASS I | Systane Lubricant Eye Drops, Ultra PF, Sterile, 25 Vials Each) recalled | Alcon Research | Sterility | Nationwide |
| Drug | CLASS III | Diphenhydramine HCl 50 mg per, Akron Pharma recalled | Akron Pharma | Other | Nationwide |
| Drug | CLASS III | Diphenhydramine HCl 25 mg per, Akron Pharma recalled | Akron Pharma | Other | Nationwide |
| Drug | CLASS II | Clobazam Tablets, 10 mg recalled by Amerisource Health ServicesClobazam | Amerisource Health Services | Packaging Defects | Nationwide |
| Drug | CLASS III | Acetaminophen per, Akron Pharma recalled | Akron Pharma | Other | Nationwide |
| Drug | CLASS II | glipiZIDE, Extended-Release Tablets, 2.5 mg ( blister cards) recalled | Amerisource Health Services | Potency & Assay | Nationwide |
| Food | CLASS I | Ready-To-Eat Frozen Drunken Chicken Product recalled | Custom Food Solutions | Undeclared Egg | |
| Food | CLASS I | Cucumber Diced recalled by First Quality Produce | First Quality Produce | Salmonella | CA |
| Food | CLASS III | Eclectic Herb Vitamin Herb Blend vita biotic dietary recalledEclectic Herb | Eclectic Institute | Foreign Material | Nationwide |
| Food | CLASS II | Yu Yee, Five Spice Powder recalled by Summit ImportYu Yee | Summit Import | Lead & Heavy Metals | 15 states |
| Food | CLASS I | Wicklow Gold Cheddar Nettle & Chive Cheese recalledWicklow Gold | Abbey Specialty Foods | Listeria | CO, MA, OH |
| Food | CLASS I | Small Veggie Platter recalled by The Kroger | The Kroger | Salmonella | 7 states |
| Food | CLASS I | Cucumber Spear recalled by First Quality Produce | First Quality Produce | Salmonella | CA |
| Food | CLASS I | Daily Veggies Enoki Mushroom recalled by New Age InternationalDaily Veggies | New Age International | Listeria | MD, NY |
| Food | CLASS I | Boar's Head Hummus Veg Platter Med recalled by The KrogerBoar's Head | The Kroger | Salmonella | 7 states |
| Food | CLASS I | Deli Fresh Vegetable Tray Med recalled by The KrogerDeli | The Kroger | Salmonella | 7 states |
| Food | CLASS I | Cucumber Coins (sliced cucumbers) recalled by First Quality Produce | First Quality Produce | Salmonella | CA |
| Food | CLASS I | Cucumbers, Wholesale Produce Supply, 752 Kasota Circle recalledCucumbers | Wholesale Produce Supply | Salmonella | 9 states |
| Food | CLASS I | Plant Protein, Complete Protein Powder Prebiotic +Fiber recalledOrgain | Orgain | Undeclared Peanuts | CA |
| Food | CLASS I | Pinsarella Roman Pizza, POL127 recalledPinsarella Roman | Pinsarella Food | Undeclared Allergens | CA |
| Food | CLASS I | Boar's Head Hummus Veg Platter Sm recalled by The KrogerBoar's Head | The Kroger | Salmonella | 7 states |
| Food | CLASS I | Wicklow Gold Cheddar Tomato & Herb recalled by Abbey Specialty FoodsWicklow Gold | Abbey Specialty Foods | Listeria | CO, MA, OH |
| Food | CLASS II | El Gallo Jalape¿o Queso salsa recalled by Las Delicias DistributorsEl Gallo | Las Delicias Distributors | Other | TX |
| Food | CLASS I | Cucumber Coins (sliced cucumbers) recalled by First Quality Produce | First Quality Produce | Salmonella | CA |
| Food | CLASS I | 14019 Cucumber Select, 01034 Cucumber Select 5# recalled | Hardies Fresh Foods | Salmonella | TX |
| Device | CLASS II | Smaxel Fractional CO2 Laser, a Class IV medical laser system recalled | IDS | Device Malfunction | Nationwide |
| Device | CLASS II | Dialyzer Optiflux 160NRe recalled by Fresenius Medical Care | Fresenius Medical Care Holdings | Packaging Defects | Nationwide |
| Device | CLASS II | AMT Mini Enteral Extension Set recalled by Applied Medical Technology | Applied Medical Technology | Other | 18 states |
| Device | CLASS I | Vasoview Hemopro 2 (w/Vasoshield) Endoscopic Vessel recalled | Maquet Cardiovascular | Other | Nationwide |
| Device | CLASS II | Tec 820 SEV Anesthesia Vaporizer, Reference Number 1177-9820-SEV recalled | GE Medical Systems | Other | Nationwide |
| Device | CLASS I | VasoView HemoPro 2 Endoscopic Vessel Harvesting System recalled | Maquet Cardiovascular | Other | Nationwide |
| Device | CLASS II | 100v Neptune 3 Rover Japanese recalled by Stryker | Stryker | Device Malfunction | GA, IL, WA |
| Device | CLASS II | Tec 850 ISO Anesthesia Vaporizer, Reference Number 1177-9850-ISO recalled | GE Medical Systems | Other | Nationwide |
| Device | CLASS II | Tec 6 Plus Anesthesia Vaporizer recalled by GE Medical Systems | GE Medical Systems | Other | Nationwide |
| Device | CLASS II | Xhibit Telemetry Receiver recalled by Spacelabs Healthcare | Spacelabs Healthcare | Device Malfunction | 27 states |
| Device | CLASS I | JMC5A Ni/TruAire-5 Oxygen Concentrator recalled | Jiangsu Jumao X-care Medical Equipment | Other | OH |
| Device | CLASS II | GE Healthcare Optima XR240amx, Mobile Digital Radiographic System recalled | GE Medical Systems | Device Malfunction | WI |
| Device | CLASS II | Vacuette Safelink recalled by Greiner Bio-One | Greiner Bio-One | Foreign Material | Nationwide |
| Device | CLASS II | Citric Complete - Dry Citric Acid Concentrate recalled | Nipro Renal Soultions USA | Labeling Errors | 10 states |
| Device | CLASS II | The EnVisio Patient Pad Transition Cushion is a component recalled | Elucent Medical | Other | 17 states |
| Device | CLASS II | Ultrasoft Oxygen Cannula, 12 Foot recalled by 3B Medical | 3B Medical | Other | AR, MA |
| Device | CLASS II | Xhibit Telemetry Receiver recalled by Spacelabs Healthcare | Spacelabs Healthcare | Device Malfunction | 44 states |
| Device | CLASS III | The FastPack IP Sex Hormone Binding Globulin Immunoassay recalled | Qualigen | Potency & Assay | 15 states |
| Device | CLASS II | VivAer Stylus recalled by Aerin Medical | Aerin Medical | Other | Nationwide |
| Device | CLASS I | Ivenix Infusion System (IIS), Large Volume Pump recalled | Fresenius Kabi USA | Device Malfunction | 6 states |
| Device | CLASS II | GE Healthcare Optima XR200amx, Mobile Digital Radiographic System recalled | GE Medical Systems | Device Malfunction | WI |
| Device | CLASS II | GE Healthcare Optima XR220amx, Mobile Digital Radiographic System recalled | GE Medical Systems | Device Malfunction | WI |
| Device | CLASS II | Access Intact PTH assay, a paramagnetic particle recalled | Beckman Coulter | Labeling Errors | Nationwide |
| Device | CLASS II | Tec 820 ISO Anesthesia Vaporizer, Reference Number 1177-9820-ISO recalled | GE Medical Systems | Other | Nationwide |
| Drug | CLASS II | Duloxetine Delayed-Release Capsules USP 20 mg recalled | Rising Pharma Holding | Nitrosamine Impurity | Nationwide |
| Drug | CLASS I | Clonazepam Orally Disintegrating Tablets, USP, 0.25 mg, C-IV recalledClonazepam | Endo USA | Labeling Errors | Nationwide |
| Drug | CLASS II | Metformin Hydrochloride Extended-Release Tablets, USP, 500 mg recalledMetformin Er 500 Mg | Granules Pharmaceuticals | Other | OH |
| Drug | CLASS I | Clonazepam Orally Disintegrating Tablet, USP, 2 mg, C-IV recalledClonazepam | Endo USA | Labeling Errors | Nationwide |
| Drug | CLASS II | Duloxetine DR Capsules USP 60 mg, a) recalled by Rising Pharma Holding | Rising Pharma Holding | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Clobazam Tablets, 10 mg recalled by Amerisource Health ServicesClobazam | Amerisource Health Services | Packaging Defects | Nationwide |
| Drug | CLASS II | medroxyPROGESTERone Acetate Injectable Suspension, USP, 150mg per mL recalledMedroxyprogesterone Acetate | Eugia US | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS III | Methadone Hydrochloride Tablets, USP, 5mg, Unit-Dose Tablets recalledMethadone Hydrochloride | West-Ward Columbus | Other | Nationwide |
| Drug | CLASS I | Clonazepam Orally Disintegrating Tablets, USP, 1 mg, C-IV recalledClonazepam | Endo USA | Labeling Errors | Nationwide |
| Drug | CLASS I | Nhan Sam Tuyet Lien Truy Phong Hoan, Capsules recalled by Buy-Herbal | Buy-Herbal | Labeling Errors | Nationwide |
| Drug | CLASS II | Duloxetine Delayed-Release Capsules USP 30 mg, a) recalled | Rising Pharma Holding | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Kit for the Preparation of Technetium Tc 99m Sulfur Colloid recalled | Jubilant Draximage Inc | Potency & Assay | Nationwide |
| Drug | CLASS II | Progesterone Injection USP, 500mg per (50mg/mL) Multiple Dose Vial recalledProgesterone | Eugia US | Particulate Matter | Nationwide |
| Drug | CLASS II | Colchicine Capsules 0.6 mg recalled by Granules PharmaceuticalsColchicine | Granules Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Ciprofloxacin Ophthalmic Solution USP, 0.3% as base recalled by FDCCiprofloxacin | FDC | Packaging Defects | Nationwide |
| Drug | CLASS I | Clonazepam Orally Disintegrating Tablets, USP, 0.125 mg, C-IV recalledClonazepam | Endo USA | Labeling Errors | Nationwide |
| Food | CLASS I | Grecian Delight Tzatziki sauce tub recalled by Grecian Delight/KronosGrecian Delight | Grecian Delight/Kronos | Salmonella | 24 states |
| Food | CLASS I | 01035 Cucumber Sliced 5# trays with sealed film recalledTexas Harvest | Dairyland Produce | Salmonella | TX |
| Food | CLASS II | Wellsley Farm Vanilla Non-fat Greek Yogurt recalled by HP Hood (VERNON)Wellsley | HP Hood (VERNON) | Foreign Material | CT, KY, MD |
| Food | CLASS I | 235214 Baker's Source Traditional Cornbread Mix Complete recalled | C.H. Guenther & Son | Undeclared Egg | 8 states |
| Food | CLASS II | Connie's Classic Thin Crust Cheese Pizza, Chicago's Finest recalledConnie's | Palermo Villa | Foreign Material | IL, MN, WI |
| Food | CLASS II | Wellsley Farm Plain Non-fat Greek Yogurt recalled by HP Hood (VERNON)Wellsley | HP Hood (VERNON) | Foreign Material | CT, KY, MD |
| Food | CLASS I | US Foods Chef's Line Greek Yogurt Tzatziki tub recalled | Grecian Delight/Kronos | Salmonella | 24 states |
| Food | CLASS I | Grecian Dip Tzatziki sauce recalled by Olympia FoodsOlympia | Olympia Foods | Salmonella | 12 states |
| Food | CLASS II | Chow Ciao Whole Grain Breaded Broccoli Nuggets recalled by Better BrandsChow Ciao | Better Brands | Foreign Material | NY |
| Food | CLASS II | Great Value, Chicken Broth , Aseptic, 6 retail units/pallet recalledGreat | Tree House Foods | Mold | AL, AR |
| Food | CLASS I | Nick The Greek Spicy Yogurt Pail recalled by Grecian Delight/KronosNick | Grecian Delight/Kronos | Salmonella | 24 states |
| Food | CLASS I | Ready-To-Eat and Raw Sausage Products recalled by UP Products | UP Products | Undeclared Soy | |
| Food | CLASS I | Frozen Chicken And Cheese Taquito Products recalled | Bestway Sandwiches | Foreign Material | |
| Device | CLASS II | Medline custom medical procedure kits labeled as: Panendoscopy-lf recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Transbond Plus Self-Etching Primer recalled by 3M Unitek | 3M Unitek | Device Malfunction | Nationwide |
| Device | CLASS II | SynchroMed II recalled by Medtronic Neuromodulation | Medtronic Neuromodulation | Device Malfunction | Nationwide |
| Device | CLASS II | Medline custom medical procedure kits labeled as recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | See DocMan recalled by MEDLINE INDUSTRIES, LP | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | SynchroMed II recalled by Medtronic Neuromodulation | Medtronic Neuromodulation | Device Malfunction | Nationwide |
| Device | CLASS II | See DocMan recalled by MEDLINE INDUSTRIES, LP | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Medline custom medical procedure kits labeled as recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Medline custom medical procedure kits labeled as recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Baxter Sigma Spectrum Infusion Pump with Master Drug Library recalled | Baxter Healthcare | Other | Nationwide |
| Device | CLASS II | Medline custom medical procedure kits labeled as recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Ivalon Anatomical Nasal Packing with Airway Tube recalled by Carwild | Carwild | Sterility | 5 states |
| Device | CLASS II | Medline custom medical procedure kits labeled as: Nasal Pack recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Baxter Sigma Spectrum Infusion Pump with Master Drug Library recalled | Baxter Healthcare | Other | Nationwide |
| Device | CLASS II | Ivalon Eye Wick- Intended to be used for the removal recalled by Carwild | Carwild | Sterility | 5 states |
| Device | CLASS II | Medline custom medical procedure kits labeled as recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Medline custom medical procedure kits labeled as recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Medline custom medical procedure kits labeled as: Cath Lab Pack-lf recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Auryon Laser System 100-120 Vac recalled by Angiodynamics | Angiodynamics | Other | Nationwide |
| Device | CLASS II | SUC-4300S, Rigid Intracardiac Sucker Fluted Tip recalled | Med Michigan Holding | Sterility | IL |
| Device | CLASS II | SynchroMed II recalled by Medtronic Neuromodulation | Medtronic Neuromodulation | Device Malfunction | Nationwide |
| Device | CLASS II | Ivalon Cellulose Surgical Spear- Intended To Be Used During recalled | Carwild | Sterility | 5 states |
| Device | CLASS II | Medline custom medical procedure kits labeled as: VP Shunt CDS recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | SynchroMed II recalled by Medtronic Neuromodulation | Medtronic Neuromodulation | Device Malfunction | Nationwide |
| Device | CLASS II | Medline custom medical procedure kits labeled as recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | See DocMan recalled by MEDLINE INDUSTRIES, LP | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Medline custom medical procedure kits labeled as: Cervical Pack-lf recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Medline custom medical procedure kits labeled as: Ensemble Rachis-lf recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Medline custom medical procedure kits labeled as recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Drug | CLASS III | Polyvinyl Alcohol Ophthalmic Solution recalled by AvKAREPolyvinyl Alcohol | AvKARE | Packaging Defects | Nationwide |
| Drug | CLASS II | Dapsone Gel recalled by Viona PharmaceuticalsDapsone | Viona Pharmaceuticals | Packaging Defects | Nationwide |
| Drug | CLASS III | Atropine Sulfate Ophthalmic Solution recalled by Somerset TherapeuticsAtropine Sulfate | Somerset Therapeutics | Potency & Assay | Nationwide |
| Drug | CLASS II | phenylephrine in 0.9% Sodium Chloride Inj, 1mg per (100 mcg/mL) recalled | Hikma Injectables USA | Sterility | Nationwide |
| Drug | CLASS I | Force Forever 400mg Tablets recalled by GNMart | GNMart | Hidden Drug Ingredients | Nationwide |
| Drug | CLASS II | ketamine inj 50 mg recalled by Hikma Injectables USA | Hikma Injectables USA | Sterility | Nationwide |
| Drug | CLASS II | Levothyroxine Sodium Tablets, Lupin, 75 mcg (0.075mg) recalledLevothyroxine Sodium | Lupin Pharmaceuticals | Potency & Assay | OH |
| Drug | CLASS II | Nitrofurantoin Capsules, USP, 100 mg Dose recalled by AvKARE | AvKARE | Potency & Assay | Nationwide |
| Drug | CLASS II | Dapsone Gel recalled by Viona PharmaceuticalsDapsone | Viona Pharmaceuticals | Packaging Defects | Nationwide |
| Drug | CLASS III | Carboxymethylcellulose Sodium Ophthalmic Solution recalled by AvKARECarboxymethylcellulose Sodium | AvKARE | Packaging Defects | Nationwide |
| Food | HEALTH ALERT | Chicken Empanada Products recalled by Rajbhog Foods (NJ) | Rajbhog Foods (NJ) | Undeclared Milk | |
| Food | CLASS I | Organic Baby Carrots --- Orangic Baby Peeled Carrots 13/3 recalled | Grimmway Enterprises | E. coli | 41 states |
| Food | CLASS II | Chocolate Raspberry: Three sizes, Small recalled by Lithuanian Bakery | Lithuanian Bakery | Undeclared Peanuts | 7 states |
| Food | CLASS II | a.) King Kullen brand Mirepoix recalled by Gracie's KitchensKing Kullen | Gracie's Kitchens | Listeria | CT, NY |
| Food | CLASS I | Crazy Fresh Turkey Havarti Wrap recalled by Russ Davis WholesaleCrazy | Russ Davis Wholesale | Salmonella | 11 states |
| Food | CLASS II | a.) King Kullen brand Vegetable Platter recalled by Gracie's KitchensKing Kullen | Gracie's Kitchens | Listeria | CT, NY |
| Food | CLASS II | a.) Gracie's Kitchen brand Mango & Blueberry Cup recalled | Gracie's Kitchens | Listeria | CT, NY |
| Food | CLASS II | a.) King Kullen brand Honeydew Slices recalled by Gracie's KitchensKing Kullen | Gracie's Kitchens | Listeria | CT, NY |
| Food | CLASS II | a.) King Kullen brand Halo Bowl recalled by Gracie's KitchensKing Kullen | Gracie's Kitchens | Listeria | CT, NY |
| Food | CLASS II | a.) King Kullen brand Diced Celery recalled by Gracie's KitchensKing Kullen | Gracie's Kitchens | Listeria | CT, NY |
| Food | CLASS I | Organic Baby Carrots --- Organic Baby Peeled Carrots Steam-to-Serve recalled | Grimmway Enterprises | E. coli | 41 states |
| Food | CLASS I | Organic Whole Carrots --- Organic Clip Carrots Cal-Organic Farm recalled | Grimmway Enterprises | E. coli | 41 states |
| Food | CLASS II | a.) King Kullen brand Mixed Fruit recalled by Gracie's KitchensKing Kullen | Gracie's Kitchens | Listeria | CT, NY |
| Food | CLASS I | whole fresh American cucumbers recalled by Baloian Farms | Baloian Farms | Salmonella | 18 states |
| Food | CLASS II | MN Milk Bank for Babies Pasteurize Donor Human Milk recalled | Minnesota Milk Bank for Babies | Foreign Material | MN |
| Food | CLASS III | An Pan bun is a sweet roll filled with sweet red bean paste recalledAn Pan | Oyatsupan Bakers | Undeclared Sesame | OR, WA |
| Food | CLASS II | a.) King Kullen brand Peppers & Onions recalled by Gracie's KitchensKing Kullen | Gracie's Kitchens | Listeria | CT, NY |
| Food | CLASS I | Garden Salad w/Ranch Dressing recalled by Russ Davis WholesaleGarden | Russ Davis Wholesale | Salmonella | 11 states |
| Food | CLASS II | a.) King Kullen brand Pineapple Slices recalled by Gracie's KitchensKing Kullen | Gracie's Kitchens | Listeria | CT, NY |
| Food | CLASS II | a.) King Kullen brand Fruit Tray recalled by Gracie's KitchensKing Kullen | Gracie's Kitchens | Listeria | CT, NY |
| Food | CLASS I | Organic Whole Carrots --- Organic Carrot 125/6 Cal-Organic Farms recalled | Grimmway Enterprises | E. coli | 41 states |
| Food | CLASS II | a.) King Kullen brand Papaya Chunks recalled by Gracie's KitchensKing Kullen | Gracie's Kitchens | Listeria | CT, NY |
| Food | CLASS II | a.) King Kullen brand Large Fruit Platter recalled by Gracie's KitchensKing Kullen | Gracie's Kitchens | Listeria | CT, NY |
| Food | CLASS II | a.) King Kullen brand Diced White Onion recalled by Gracie's KitchensKing Kullen | Gracie's Kitchens | Listeria | CT, NY |
| Food | CLASS I | Napoleonas Torte packaged under the following sizes: Small recalledNapoleonas Torte | Lithuanian Bakery | Undeclared Milk | 7 states |
| Food | CLASS II | a.) King Kullen brand Mango Berry recalled by Gracie's KitchensKing Kullen | Gracie's Kitchens | Listeria | CT, NY |
| Food | CLASS I | Whole and Cut Cucumbers recalled by Russ Davis Wholesale | Russ Davis Wholesale | Salmonella | 11 states |
| Food | CLASS II | a.) King Kullen brand Brussel Sprout Halves recalledKing Kullen | Gracie's Kitchens | Listeria | CT, NY |
| Food | CLASS II | a.) King Kullen brand Fajita Mix recalled by Gracie's KitchensKing Kullen | Gracie's Kitchens | Listeria | CT, NY |
| Food | CLASS I | FCF Item 404885, Gyro Kit No Trays. Each box consists of 2/5.25lbs. recalledFCF Item | Reser's Fine Foods | Salmonella | 19 states |
| Food | CLASS II | a.) Wild by Nature brand Fruit Spears recalled by Gracie's Kitchensby Nature | Gracie's Kitchens | Listeria | CT, NY |
| Food | CLASS II | a.) WIld by Nature brand Squash Noodles recalled by Gracie's Kitchensby Nature | Gracie's Kitchens | Listeria | CT, NY |
| Food | CLASS II | a.) Wild by Nature brand Sliced Mixed Peppers recalledby Nature | Gracie's Kitchens | Listeria | CT, NY |
| Food | CLASS II | a.) King Kullen brand Stuffed Artichokes recalled by Gracie's KitchensKing Kullen | Gracie's Kitchens | Listeria | CT, NY |
| Food | CLASS II | Member's Mark Hatch Chile Chicken Enchiladas, ready to cook recalledMember's Mark | Sam'S Club | Listeria | Nationwide |
| Food | CLASS II | Wegmans Jalapeno Baked Cheese Puffs, Jalapeno flavored recalledWegmans | Herr Foods | Undeclared Allergens | NY |
| Food | CLASS II | a.) King Kullen brand Tri Colored Noodles recalled by Gracie's KitchensKing Kullen | Gracie's Kitchens | Listeria | CT, NY |
| Food | CLASS I | Cappuccino Meltaway Bar recalled by Gardner's CandiesGardner's Candies | Gardner's Candies | Undeclared Tree Nuts | 11 states |
| Food | CLASS II | a.) King Kullen brand Mango recalled by Gracie's KitchensKing Kullen | Gracie's Kitchens | Listeria | CT, NY |
| Food | CLASS II | a.) Gracie's Kitchen brand Diced Carrots recalled | Gracie's Kitchens | Listeria | CT, NY |
| Food | CLASS II | a.) King Kullen brand Watermelon Slices recalled by Gracie's KitchensKing Kullen | Gracie's Kitchens | Listeria | CT, NY |
| Food | CLASS I | Bacon Avocado Wrap recalled by Russ Davis Wholesale | Russ Davis Wholesale | Salmonella | 11 states |
| Food | CLASS II | a.) King Kullen brand Tropical Delight Bowl recalledKing Kullen | Gracie's Kitchens | Listeria | CT, NY |
| Food | CLASS II | a.) King Kullen brand Cantaloupe Slices recalled by Gracie's KitchensKing Kullen | Gracie's Kitchens | Listeria | CT, NY |
| Food | CLASS II | a.) King Kullen brand Watermelon Halo recalled by Gracie's KitchensKing Kullen | Gracie's Kitchens | Listeria | CT, NY |
| Food | CLASS I | Product is a whole, fresh cucumber recalled by Delta FreshProduct | Delta Fresh | Salmonella | 8 states |
| Food | CLASS II | a.) Gracie's Kitchen brand Broccoli Florets recalled | Gracie's Kitchens | Listeria | CT, NY |
| Food | CLASS II | a.) King Kullen brand Fiesta Watermelon Bowl recalledKing Kullen | Gracie's Kitchens | Listeria | CT, NY |
| Food | CLASS II | a.) Gracie's Kitchen brand Cauliflower Florets recalled | Gracie's Kitchens | Listeria | CT, NY |
| Food | CLASS II | a.) Gracie's Kitchen brand Broccoli & Cauliflower Florets recalled | Gracie's Kitchens | Listeria | CT, NY |
| Food | CLASS II | a.) King Kullen brand Fiesta Bowl recalled by Gracie's KitchensKing Kullen | Gracie's Kitchens | Listeria | CT, NY |
| Food | CLASS II | a.) King Kullen brand Diced Red Onion recalled by Gracie's KitchensKing Kullen | Gracie's Kitchens | Listeria | CT, NY |
| Food | CLASS I | Sprout Gyro Family Kit recalled by Sprouts Farmers MarketSprout Gyro | Sprouts Farmers Market | Salmonella | 24 states |
| Food | CLASS I | FCF Item 404884, Gyro Kit With Trays. Each tray consists recalledFCF Item | Reser's Fine Foods | Salmonella | 19 states |
| Food | CLASS I | Cascade Raw Cheddar recalled by Heber Valley Artisan CheeseCascade | Heber Valley Artisan Cheese | E. coli | 4 states |
| Food | CLASS II | a.) King Kullen brand Tropical Fruit Cup recalled by Gracie's KitchensKing Kullen | Gracie's Kitchens | Listeria | CT, NY |
| Food | CLASS I | Kowalski's Garden Salad recalled by Russ Davis WholesaleKowalski's Garden | Russ Davis Wholesale | Salmonella | 11 states |
| Food | CLASS I | Organic Baby Carrots --- Organic Baby Carrots 25 Grimmway Farms recalled | Grimmway Enterprises | E. coli | 41 states |
| Food | CLASS I | Beef & Lamb Gyro Sandwich Express Meal Kit recalled | Reser's Fine Foods | Salmonella | 19 states |
| Food | HEALTH ALERT | Frozen, Raw Ground Beef Products recalled by Stockyards Packing | Stockyards Packing | Foreign Material | |
| Device | CLASS I | StatStrip Glucose Ketone Hospital Meter System recalled | Nova Biomedical | Device Malfunction | Nationwide |
| Device | CLASS II | Device Description: FACSLyric 2L6C Instrument US recalled | Becton, Dickinson and Company, BD Bio Sciences | Device Malfunction | Nationwide |
| Device | CLASS II | Daytona Small Stature Ti Locking Cap, Small Stature, T25 recalled | Seaspine Orthopedics | Device Malfunction | Nationwide |
| Device | CLASS II | epoc NXS Host recalled by Siemens Healthcare Diagnostics | Siemens Healthcare Diagnostics | Device Malfunction | Nationwide |
| Device | CLASS II | epoc NXS Host recalled by Siemens Healthcare Diagnostics | Siemens Healthcare Diagnostics | Device Malfunction | Nationwide |
| Device | CLASS II | FACSLyric 3L8C Instrument Us-ivd recalled by Becton, Dickinson and | Becton, Dickinson and Company, BD Bio Sciences | Device Malfunction | Nationwide |
| Device | CLASS II | Medline medical procedure convenience kits, labeled as recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | ST IUD Removal Hook 10" (504090), Medline recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Major Neuro Pack-lf Convenience kit recalled by MEDLINE INDUSTRIES, LP | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | FACSLyric 3L10C Instrument Us-ivd recalled by Becton, Dickinson and | Becton, Dickinson and Company, BD Bio Sciences | Device Malfunction | Nationwide |
| Device | CLASS II | epoc NXS Host recalled by Siemens Healthcare Diagnostics | Siemens Healthcare Diagnostics | Device Malfunction | Nationwide |
| Device | CLASS II | FACSLyric 3L12C Instrument RUO recalled by Becton, Dickinson and | Becton, Dickinson and Company, BD Bio Sciences | Device Malfunction | Nationwide |
| Device | CLASS II | Soft Touch II Surgical Mask, Blue-Disposable surgical mask recalled | O&M Halyard | Packaging Defects | Nationwide |
| Device | CLASS II | Sterile Strt Kelly Hemostat (SK8039S), Medline recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | FACSLyric 2L4C Instrument US recalled by Becton, Dickinson and | Becton, Dickinson and Company, BD Bio Sciences | Device Malfunction | Nationwide |
| Device | CLASS II | LINK MP Reconstruction System Neck Segment recalled | Waldemar Link GmbH & Co. KG (Mfg Site) | Other | Nationwide |
| Device | CLASS II | Rummell, Medline recalled by MEDLINE INDUSTRIES, LP | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS I | Monitoring Service Application (MSA) recalled by Braemar Manufacturing | Braemar Manufacturing | Device Malfunction | Nationwide |
| Device | CLASS II | Medline medical procedure convenience kits, labeled as recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Misha Knee System Implant Small, Left recalled by Moximed | Moximed | Device Malfunction | Nationwide |
| Device | CLASS II | Medline medical procedure convenience kits, labeled as: Sinus recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Medline medical procedure convenience kits, labeled as recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | TEMA Elbow - Axle Small recalled by Limacorporate S.p.A | Limacorporate | Other | FL, TX |
| Device | CLASS II | 20/30 Priority Pack Kit/.115 RHV recalled by Abbott Vascular | Abbott Vascular | Packaging Defects | 40 states |
| Device | CLASS II | Procedure Mask with SO SOFT* Earloops recalled by O&m Halyard | O&M Halyard | Packaging Defects | Nationwide |
| Device | CLASS II | epoc NXS Host recalled by Siemens Healthcare Diagnostics | Siemens Healthcare Diagnostics | Device Malfunction | Nationwide |
| Device | CLASS II | 20/30 Indeflator, REF: 1000184, for use during cardiovascular recalled | Abbott Vascular | Packaging Defects | 40 states |
| Device | CLASS II | Fess-mb Pack-lf Convenience kit recalled by MEDLINE INDUSTRIES, LP | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | epoc NXS Host recalled by Siemens Healthcare Diagnostics | Siemens Healthcare Diagnostics | Device Malfunction | Nationwide |
| Device | CLASS II | Diep Flap Convenience kit recalled by MEDLINE INDUSTRIES, LP | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | O.R. Scissors, S/B, 5.5 Sterile, Medline recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | epoc NXS Host recalled by Siemens Healthcare Diagnostics | Siemens Healthcare Diagnostics | Device Malfunction | Nationwide |
| Device | CLASS II | Galaxy System (GAL-001) recalled by Noah Medical | Noah Medical | Device Malfunction | 15 states |
| Device | CLASS II | Empowr 3D Knee Tibial Insert, 6R, VE recalled by Encore Medical | Encore Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Medline medical procedure convenience kits, labeled as: Craniotomy recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Clarity Precision Grip Attachments, for use in orthodontic treatment recalled | 3M Company - Health Care Business | Device Malfunction | Nationwide |
| Device | CLASS II | Panther Fusion Sars-CoV-2/Flu A/B/RSV Assay recalled by Hologic | Hologic | Potency & Assay | AK |
| Device | CLASS I | StatStrip Glucose Ketone (mmol/L) Hospital Meter System recalled | Nova Biomedical | Device Malfunction | Nationwide |
| Device | CLASS II | epoc NXS Host recalled by Siemens Healthcare Diagnostics | Siemens Healthcare Diagnostics | Device Malfunction | Nationwide |
| Device | CLASS II | Empowr 3D Knee Tibial Insert, 5R, VE recalled by Encore Medical | Encore Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Sterile Magill Forcep (MAGF9), Medline recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | epoc NXS Host recalled by Siemens Healthcare Diagnostics | Siemens Healthcare Diagnostics | Device Malfunction | Nationwide |
| Device | CLASS I | StatStrip Glucose Hospital Meter System recalled by Nova Biomedical | Nova Biomedical | Device Malfunction | Nationwide |
| Device | CLASS II | ST OR Mayo Hegar Needleholder 6"(OR2500), Medline recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | 20/30 Priority Pack Accessory Kit/.096 RHV recalled by Abbott Vascular | Abbott Vascular | Packaging Defects | 40 states |
| Device | CLASS II | Access hsTnI Reagent recalled by Beckman Coulter | Beckman Coulter | Potency & Assay | MN |
| Device | CLASS II | Septoplasty Pack Convenient kit recalled by MEDLINE INDUSTRIES, LP | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Magnesium Flex reagent cartridge, 360 tests recalled | Siemens Healthcare Diagnostics | Device Malfunction | Nationwide |
| Device | CLASS II | KIT,Spine LH Convenience kit recalled by MEDLINE INDUSTRIES, LP | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Daytona Small Stature CoCr LockingCap, Small Stature, T25, BT recalled | Seaspine Orthopedics | Device Malfunction | Nationwide |
| Device | CLASS II | ST Reprocessed Bruns Curette #00 (BC00), Medline recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | 20/30 Priority Pack Accessory Kit w/Copilot recalled by Abbott Vascular | Abbott Vascular | Packaging Defects | 40 states |
| Drug | CLASS II | Duloxetine Delayed-Release Capsules, USP, 60 mg recalled | Amerisource Health Services | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Duloxetine Delayed-Release Capsules, USP, 60 mg recalledDuloxetine | Breckenridge Pharmaceutical | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Umary Acid Hyaluronic, 850 MG Caplets, Upc7502265120323 recalled | Mxbbb | Labeling Errors | TX |
| Drug | CLASS II | DULoxetine DR USP, 30 mg recalled by PD-Rx Pharmaceuticals | PD-Rx Pharmaceuticals | Nitrosamine Impurity | FL, MS, WI |
| Drug | CLASS II | chlorproMAZINE Hydrochloride Tablets, USP, 25 mg recalledChlorpromazine Hydrochloride | Glenmark Pharmaceuticals Inc., USA | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Duloxetine Delayed-Release Capsules USP, 60 mg recalled | Amerisource Health Services | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Duloxetine Delayed-Release Capsules, 60 mg, a) blister cards recalled | RemedyRepack | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Duloxetine Delayed-Release Capsules USP, 30 mg recalled | Amerisource Health Services | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Duloxetine Delayed-Release Capsules, USP, 30 mg recalled | Amerisource Health Services | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Kit for the Preparation of Technetium Tc 99m Sestamibi recalledTechnetium Tc 99m Sestamibi | Curium US | Sterility | Nationwide |
| Drug | CLASS II | chlorproMAZINE Hydrochloride Tablets, USP, 10mg recalledChlorpromazine Hydrochloride | Glenmark Pharmaceuticals Inc., USA | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Duloxetine Delayed-Release Capsules, USP, 30mg recalledDuloxetine | Breckenridge Pharmaceutical | Nitrosamine Impurity | Nationwide |
| Food | CLASS II | ZOE Daily 30+ Prebiotic blend recalled by Zoe USZoe | Zoe US | Foreign Material | 26 states |
| Food | CLASS I | Raw cucumbers recalled by SunFed Produce | SunFed Produce | Salmonella | Nationwide |
| Food | CLASS I | Cucumber Diced Greek Cut (1/8"x1/8"x1"), 360# Drum with poly liner recalled | E-z Spuds | Salmonella | IL |
| Food | CLASS I | Kirkland Signature Organic Eggs Pasture-raised 24 Eggs recalledKirkland Signature | Handsome Brook Farms | Salmonella | 5 states |
| Food | CLASS II | Borsari Food Company Incorporated; Bloody Mary MIX ; 32 FL. OZ recalledBorsari | Borsari Food Company | Undeclared Fish & Shellfish | 25 states |