FDA Recalls, Food, Drug & Medical Device Alerts - Page 23 of 27
Latest food, drug, and medical device recalls issued by the U.S. Food and Drug Administration. Class I, II, and III recall classifications, affected products, and consumer guidance.
Showing 1,101–1,150 of 1,348 FDA recalls. Browse by month →
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Medline Industries Recalls 82,597 Surgical Convenience Kits Over Sterility Concerns
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Olympus Recalls High Flow Insufflation Units Due to Overpressure Risk
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Integra LifeSciences Recalls Private Label CVS Wound Care Products Over Sterility Concerns
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Medline Industries Recalls Surgical and Medical Convenience Kits Over Sterility Concerns
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Auris Health Recalls MONARCH Bronchoscopy Platform Due to Software Malfunction
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Wilson-Cook Medical Inc. Recalls Teslatome Bipolar Sphincterotomes Due to Electrical Hazard
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Medline Industries Recalls Over 926,000 IV Administration and Extension Sets Due to Connector Failure
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Medline Industries Recalls Admit Kits Due to Potential Sterility Compromise
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Medline Industries Recalls Convenience Kits Over Potential Sterility Concerns
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Olympus Corporation Recalls Thunderbeat Surgical Devices Due to Adverse Event Reports
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Medline Industries Recalls Drape Pack-Choice Convenience Kits Over Sterility Concerns
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Olympus Recalls Thunderbeat Surgical Devices Following Reports of Adverse Events
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Medline Industries Recalls Convenience Kits Due to Potential Sterility Concerns
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Integra LifeSciences Recalls MediHoney Gel Due to Potential Sterile Barrier Breach
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Bard Peripheral Vascular Recalls Hickman and Broviac Catheter Trays Over Sterility Risks
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Medline Recalls Triple Lumen Insertion Kits Over Sterilization Equipment Calibration Issues
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Immunotech A.S. Issues Recall for Estrone RIA Kits Over Inaccurate Test Results
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Woodland Foods LLC Recalls Woodland Gourmet Arrowroot Flour Due to Foreign Material
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Lotus Mom Corporation Recalls Brass Tope Over Potential Lead Contamination
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H & N Group Inc. Recalls Frozen Cooked Shrimp Due to Potential Cesium-137 Contamination
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Reser's Fine Foods Recalls Molly Kitchen's Tuna Salad Due to Undeclared Fish Allergen
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Pure Solutions, Inc. Recalls Sleep Supplements Due to Undeclared Milk Allergen
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Why Not Natural Moringa Capsules Recalled Due to Potential Salmonella Contamination
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Philips North America Recalls Spectral CT 7500 on Rails Over Potential Rotor Part Displacement
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Medline Industries Recalls Mercy Circumcision Trays Due to Compromised Packaging
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Medline Industries Recalls Reprocessed ViewFlex Xtra ICE Catheters Due to Potential Particle Contamination
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Medline Industries Recalls Adult Catheter Securement Dressing Kits Due to Packaging Defect
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Medline Industries Recalls Blood Culture Kits Over Potential Packaging Seal Breach
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Medline Industries Recalls Reprocessed Livewire Steerable Electrophysiology Catheters Due to Contamination Risk
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Medline Industries Recalls Over 21,000 Medical Kits Due to Compromised Swabstick Packaging
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Medline Industries Recalls Reprocessed Biosense Webster Ultrasound Catheters Due to Potential Contamination
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Medline Industries Recalls Sterile Resuture Packs Due to Potential Packaging Seal Defect
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Surepulse Medical Ltd Recalls VS Cap Extra Large Over Labeling Error
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Medline Industries Recalls Adult Intubation Trays Over Life-Threatening Catheter Size Error
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Surepulse Medical Ltd Recalls VS Cap Extra Small Due to Incorrect Sizing Labeling
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Philips Recalls Azurion 5 M20 Systems Due to Unexpected Table Movement Hazard
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Elekta, Inc. Recalls Leksell GammaPlan Software Over Radiation Targeting Error
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Medline Industries Recalls Medical Convenience Kits Due to BD ChloraPrep Packaging Defect
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Steris Corporation Recalls Barco MNA with HexaVue IP Integration System Due to Configuration Error
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Philips Medical Systems Recalls Azurion 7 B20 Systems Due to Unexpected Table Movement
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Medline Industries Recalls Anesthesia Artline Packs Due to Potential Packaging Defect
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SurePulse Medical Ltd Recalls Surepulse VS Cap Small Due to Labeling Error
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Medline Recalls Suture Removal Trays Due to Potential Compromise of Sterile Packaging
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Philips Medical Systems Recalls Azurion 3 M12 Systems Due to Unexpected Table Movement
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Medline Industries Recalls Reprocessed St. Jude Diagnostic Electrophysiology Catheters Due to Contamination Risk
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Straumann USA LLC Recalls WB Impression Post Closed Trays Due to Component Mix-Up
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Alphatec Spine Recalls ATEC Lateral Navigation Disc Prep Instruments Due to Design Flaw
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Philips North America Recalls IQon Spectral CT Systems Due to Loose Fastener Risk
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Philips Medical Systems Recalls Azurion 3 M15 Systems Due to Unexpected Table Movement
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AVID Medical, Inc. Recalls Halyard TRANSPORT BAG KIT Over Potential Sterility Compromise
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