FDA Recalls - March 2026 (127 reports)
FDA Recalls issued during March 2026.
March 2026 ran 44% below the trailing 12-month average of 225 reports/month.
FDA Recalls
Agiliti Health Recalls Adapt Pump Support Surfaces Due to Software Malfunction
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FDA Recalls
Medline Industries Recalls Nail Kits Due to Potential Sterility Concerns
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FDA Recalls
Edermy LLC Issues Recall for PIE Trolley System Model 2005 Due to Lack of FDA Clearance
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FDA Recalls high
Olympus Recalls Inner Sheaths Due to Risk of Ceramic Tip Breakage
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FDA Recalls
Hitachi Recalls PROBEAT-CR Proton Beam Therapy System Due to Software Anomaly
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FDA Recalls high
Medline Industries Recalls Medical Kits Containing Tego Connectors Due to Seal Defects
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FDA Recalls high
Olympus Recalls Inner Sheath Model A2642 Over Reports of Breaking Ceramic Tips
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FDA Recalls high
Medline Industries Recalls Over 10,000 Convenience Kits Due to Sterility Concerns
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FDA Recalls
Medline Recalls Over 3.5 Million Units of Sterile Saline Wound Wash Due to Sterility Concerns
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FDA Recalls
Encore Medical Recalls EMPOWR 3D KNEE Implants Due to Incorrect Labeling
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FDA Recalls
Olympus Corporation Recalls Cystoscope Outer Sheaths Due to Laser Incompatibility
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FDA Recalls
Olympus Recalls Resection Sheaths Over Ceramic Tip Breakage Risk
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FDA Recalls
Remel, Inc. Issues Recall for Campy CVA Medium Over Bacterial Recovery Concerns
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FDA Recalls
Olympus Recalls Inner Sheath 21 Fr. Model A2660T Over Ceramic Tip Breakage Concerns
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FDA Recalls
Olympus Issues Recall for Resection Sheaths Due to Risk of Ceramic Tip Breakage
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FDA Recalls
Edermy LLC Recalls PIE PAK Medical Devices Due to Lack of 510K Clearance
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FDA Recalls
Olympus Recalls Resection Inner Sheaths Due to Ceramic Tip Breakage
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FDA Recalls
Medline Industries Recalls Meijer Sterile Saline Wound Wash Over Sterility Concerns
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FDA Recalls high
Olympus Recalls Inner Sheaths Used in Gynecological Procedures Due to Breaking Ceramic Tips
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FDA Recalls
Olympus Issues Recall for Resection Sheath Due to Risk of Ceramic Tip Breakage
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FDA Recalls
Encore Medical, LP Recalls Reverse Shoulder Prosthesis (RSP) Humeral Socket Inserts Due to Labeling Error
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FDA Recalls
Olympus Recalls Resection Sheaths Over Risk of Ceramic Tip Breakage
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FDA Recalls high
Medline Industries Recalls IR Packs and Dialysis Insertion Kits Due to Faulty Tego Connectors
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FDA Recalls
Medline Industries Recalls Nail Kits Due to Potential Sterility Issues in Wound Wash
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FDA Recalls
Medtronic Recalls Octopus Nuvo Tissue Stabilizers Due to Assembly Error
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FDA Recalls
Olympus Corporation Recalls Resection Inner Sheaths Due to Ceramic Tip Breakage Risk
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FDA Recalls
Olympus Corporation of the Americas Recalls Inner Sheath Devices Due to Breaking Ceramic Tips
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FDA Recalls
Olympus Recalls Resection Sheaths Due to Risk of Ceramic Tip Breakage
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FDA Recalls high
Olympus Issues Recall for Inner Sheath Used in Urological Procedures Due to Breaking Ceramic Tips
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FDA Recalls
Olympus Corporation Recalls Resection Sheaths Due to Risk of Ceramic Tip Breakage
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FDA Recalls high
Medline Industries Recalls Over 14,000 Dialysis Kits and Trays Due to Tego Connector Seal Defects
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FDA Recalls
Olympus Recalls Inner Sheaths Used in Urological and Gynecological Procedures Due to Breakage Risk
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FDA Recalls high
MRIMed Inc. Recalls MRI LED Mobile Exam Light Batteries Due to Overheating and Smoke Hazard
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FDA Recalls
Olympus Corporation Recalls Resection Sheaths Due to Risk of Ceramic Tip Breaking
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FDA Recalls
Encore Medical, LP Recalls Reverse Shoulder Prosthesis Humeral Socket Inserts Due to Incorrect Labeling
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FDA Recalls high
Medline Industries Recalls Dialysis Dressing Change Kits Due to Tego Connector Seal Defects
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FDA Recalls high
Medline Industries Recalls Dialysis On/Off Kits Due to Tego Connector Seal Issues
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FDA Recalls high
Prime Food Processing LLC Recalls Dried Croaker Fish Due to Uneviscerated Fish Hazard
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FDA Recalls
Lubna Quality Products Inc. Recalls Mung Beans in Texas and Louisiana Due to Pesticide
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FDA Recalls
Valley Springs Artesian Gold Recalls Bottled Water Due to Insanitary Conditions
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FDA Recalls high
Oregon Potato Company Recalls IQF Blueberries Due to Listeria monocytogenes Risk
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FDA Recalls
SB FOOD LLC Recalls Yoyo Gummy Assorted Flavor Over Unallowed Color Additive
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FDA Recalls
SB FOOD LLC Recalls Yoyo Gummy Tropical Flavor Over Unapproved Color Additive
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FDA Recalls
Valley Springs Steamed Distilled Water Recall Issued Due to Insanitary Bottling Conditions
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FDA Recalls
SB FOOD LLC Recalls Yoyo Gummy Grape Plus Flavor Over Unallowed Color Additive
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FDA Recalls high
MIN JIANG FOOD STORE INC Recalls Frozen Fish Balls Due to Undeclared Wheat and Sesame
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FDA Recalls high
Wellsley Farms Farm-Raised Atlantic Salmon Recalled Due to Listeria Risk
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FDA Recalls high
Navitas Organics Recalls Organic Chia Seeds Due to Potential Salmonella Contamination
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FDA Recalls
Tengen USA Trading Corp Recalls YO!MAN Lettuce Due to Undeclared Cyclamates
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FDA Recalls
Tengen USA Trading Corp Recalls YO!MAN Cucumber Due to Undeclared Cyclamates
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FDA Recalls
Valley Springs Artesian Gold Recalls Bottled Water Over Insanitary Conditions
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FDA Recalls
Wizcure Pharmaa Recalls Fluorescein Sodium Ophthalmic Strips Over Sterility Concerns
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FDA Recalls
Agebox Recalls iKids-Growth Capsules Due to Undeclared Ibutamoren
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FDA Recalls high
Vista Meibo Tears Eye Drops Recalled Nationwide Due to Sterility Concerns
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FDA Recalls high
Agebox Recalls iKids-Growth Night Formula Due to Undeclared Ibutamoren
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FDA Recalls high
Vista Gonio Eye Lubricant Recall Issued Due to Sterility Concerns
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FDA Recalls high
LEO Pharma Inc. Recalls Adbry Injection Due to Potential Wool Fiber Contamination
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FDA Recalls high
Vista Gel Hypromellose Eye Drops Recalled Nationwide Due to Sterility Concerns
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FDA Recalls
AvKARE Issues Voluntary Recall for Amantadine HCl Capsules Due to Dissolution Failure
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FDA Recalls
Slate Run Pharmaceuticals Recalls Eptifibatide Injection Due to Labeling Error
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FDA Recalls
Wizcure Pharmaa Recalls Vista Tears Eye Drops Nationwide Over Sterility Concerns
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FDA Recalls high
Wizcure Pharmaa Recalls Bio Glo Fluorescein Sodium Ophthalmic Strips Due to Sterility Concerns
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FDA Recalls high
BioGlo Fluorescein Sodium Ophthalmic Strips Recalled Due to Sterility Concerns
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FDA Recalls
Centinel Spine Recalls Prodisc C SK Cervical Disc Replacement Devices Due to Mislabeled Sizing
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FDA Recalls
Medline Industries Recalls 154,427 Convenience Kits Over Sterility Concerns
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FDA Recalls high
Medline Industries Recalls Chest/Breast Convenience Kits Due to Sterility Concerns
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FDA Recalls
Medline Industries Recalls Over 14 Million Surgical Drapes Due to Sterility Concerns
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FDA Recalls
Medline Industries Recalls Over 117,000 Convenience Kits Due to Sterility Concerns
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FDA Recalls
Medline Industries Recalls Urology Convenience Kits Over Sterility Assurance Concerns
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FDA Recalls high
Medline Industries Recalls C-Section Convenience Kits Due to Sterility Assurance Concerns
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FDA Recalls high
Medline Industries Recalls 30,958 Convenience Kits Over Sterility Concerns
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FDA Recalls
Medline Industries Recalls Over 39,000 Convenience Kits Due to Sterility Concerns
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FDA Recalls high
Medline Industries Recalls Basic Nerve Block Trays Due to Sterilization Calibration Issues
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FDA Recalls
Intuitive Surgical Recalls Da Vinci 5 Surgical Consoles Due to Software Error
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FDA Recalls
Medline Industries Recalls Arthroscopy Kits and Trays Due to Sterility Concerns
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FDA Recalls
Medline Industries Recalls Surgical Convenience Kits Over Sterility Concerns
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FDA Recalls high
Olympus Recalls High Flow Insufflation Units Due to Software-Related Overpressure Risk
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FDA Recalls
Medline Industries Recalls 4,853 Convenience Kits Over Sterilization Calibration Issues
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FDA Recalls high
Medline Industries Recalls Dental Packs Due to Potential Sterility Issues
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FDA Recalls
Integra LifeSciences Recalls MEDIHONEY Calcium Alginate Dressings Due to Potential Sterility Breach
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FDA Recalls
Medline Industries Recalls 5,346 Medical Convenience Kits Over Sterility Concerns
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FDA Recalls high
Medica Corporation Recalls Capillary Tube Kits Due to Inaccurate Potassium Results
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FDA Recalls
Medline Industries Recalls Over 193,000 Surgical Packs Due to Sterilization Concerns
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FDA Recalls
Medline Industries Recalls Convenience Kits Over Sterility Concerns
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FDA Recalls
Stryker Corporation Recalls MOLLI 2 System Components Over Marker Dislodgement Risk
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FDA Recalls
Medline Industries Recalls Over 27,000 Convenience Kits Due to Sterility Concerns
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FDA Recalls
Medline Industries Recalls Over 70 Million Surgical Gowns Due to Sterility Concerns
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FDA Recalls high
Medline Industries Recalls 3,561 Medical Convenience Kits Over Sterility Concerns
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FDA Recalls high
Olympus Recalls Thunderbeat Surgical Devices Due to Adverse Event Reports
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FDA Recalls
Medline Industries Recalls 7,494 Neuro Convenience Kits Over Sterility Concerns
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FDA Recalls high
Medline Industries Recalls Over 4,700 Convenience Kits Due to Sterility Concerns
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FDA Recalls
Medline Recalls Convenience GI Kits Over Potential Sterility Assurance Issues
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FDA Recalls high
Medline Industries Recalls Burn Packs Over Sterilization Equipment Calibration Issues
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FDA Recalls high
Medline Industries Recalls Over 12,000 Surgical Convenience Kits Due to Sterility Concerns
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FDA Recalls high
Baxter Healthcare Recalls Spectrum IQ Infusion Pumps Due to Missing Safety Testing
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FDA Recalls
Medline Industries Recalls Convenience Kits Over Potential Sterility Assurance Issues
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FDA Recalls
Medline Industries Recalls Convenience Kits Due to Potential Sterility Assurance Issues
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FDA Recalls high
Medline Industries Recalls LVAD Driveline and Central Line Dressing Trays Over Sterility Concerns
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FDA Recalls
Medline Industries Recalls PPE Kits Due to Potential Sterility Issues
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FDA Recalls high
Olympus Recalls High Flow Insufflation Units Over Software-Related Overpressure Risk
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FDA Recalls
Medline Industries Recalls Lithotomy Packs Due to Potential Sterility Concerns
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FDA Recalls high
Medline Industries Recalls 9,051 Convenience Kits Over Sterility Assurance Concerns
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FDA Recalls high
Medline Industries Recalls Tracheostomy Convenience Kits Due to Sterility Concerns
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FDA Recalls
Medline Industries Recalls General Closure Convenience Kits Over Sterility Assurance Concerns
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FDA Recalls high
Medline Industries Recalls 82,597 Surgical Convenience Kits Over Sterility Concerns
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FDA Recalls high
Olympus Recalls High Flow Insufflation Units Due to Overpressure Risk
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FDA Recalls
Integra LifeSciences Recalls Private Label CVS Wound Care Products Over Sterility Concerns
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FDA Recalls
Medline Industries Recalls Surgical and Medical Convenience Kits Over Sterility Concerns
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FDA Recalls
Auris Health Recalls MONARCH Bronchoscopy Platform Due to Software Malfunction
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FDA Recalls high
Wilson-Cook Medical Inc. Recalls Teslatome Bipolar Sphincterotomes Due to Electrical Hazard
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FDA Recalls high
Medline Industries Recalls Over 926,000 IV Administration and Extension Sets Due to Connector Failure
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FDA Recalls high
Medline Industries Recalls Admit Kits Due to Potential Sterility Compromise
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FDA Recalls
Medline Industries Recalls Convenience Kits Over Potential Sterility Concerns
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FDA Recalls high
Olympus Corporation Recalls Thunderbeat Surgical Devices Due to Adverse Event Reports
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FDA Recalls high
Medline Industries Recalls Drape Pack-Choice Convenience Kits Over Sterility Concerns
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FDA Recalls high
Olympus Recalls Thunderbeat Surgical Devices Following Reports of Adverse Events
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FDA Recalls
Medline Industries Recalls Convenience Kits Due to Potential Sterility Concerns
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FDA Recalls high
Integra LifeSciences Recalls MediHoney Gel Due to Potential Sterile Barrier Breach
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FDA Recalls
Bard Peripheral Vascular Recalls Hickman and Broviac Catheter Trays Over Sterility Risks
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FDA Recalls high
Medline Recalls Triple Lumen Insertion Kits Over Sterilization Equipment Calibration Issues
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FDA Recalls
Immunotech A.S. Issues Recall for Estrone RIA Kits Over Inaccurate Test Results
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FDA Recalls
Woodland Foods LLC Recalls Woodland Gourmet Arrowroot Flour Due to Foreign Material
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FDA Recalls high
Lotus Mom Corporation Recalls Brass Tope Over Potential Lead Contamination
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FDA Recalls high
H & N Group Inc. Recalls Frozen Cooked Shrimp Due to Potential Cesium-137 Contamination
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FDA Recalls high
Reser's Fine Foods Recalls Molly Kitchen's Tuna Salad Due to Undeclared Fish Allergen
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FDA Recalls high
Pure Solutions, Inc. Recalls Sleep Supplements Due to Undeclared Milk Allergen
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FDA Recalls high
Why Not Natural Moringa Capsules Recalled Due to Potential Salmonella Contamination
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All federal data sources used on this page
- FDA Enforcement Report - official FDA recall classifications for food, drugs, devices, biologics, and tobacco. fda.gov/safety/recalls
- FDA Recalls, Withdrawals & Safety Alerts API - openFDA recall endpoint. open.fda.gov
- USDA Food Safety and Inspection Service (FSIS) - meat, poultry, and processed-egg-product recalls. fsis.usda.gov/recalls
- CDC Foodborne Outbreaks - outbreak investigation context for food recalls. cdc.gov/foodsafety/outbreaks
- Consumer Product Safety Commission (CPSC) - non-food consumer-product recalls cross-reference. cpsc.gov/recalls
- NHTSA Vehicle Recalls - automobile and tire recalls cross-reference. nhtsa.gov/recalls