FDA Recalls, Food, Drug & Medical Device Alerts - Page 39 of 46
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 1,901–1,950 of 2,262 FDA recalls. Browse by month →
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Medline Industries Recalls Dental Packs Due to Potential Sterility Issues
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Medline Industries Recalls Dialysis Dressing Change Kits Due to Tego Connector Seal Defects
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Medline Industries Recalls Dialysis On/Off Kits Due to Tego Connector Seal Issues
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Medline Industries Recalls Drape Pack-Choice Convenience Kits Over Sterility Concerns
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Medline Industries Recalls General Closure Convenience Kits Over Sterility Assurance Concerns
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Medline Industries Recalls IR Packs and Dialysis Insertion Kits Due to Faulty Tego Connectors
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Medline Industries Recalls Lithotomy Packs Due to Potential Sterility Concerns
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Medline Industries Recalls LVAD Driveline and Central Line Dressing Trays Over Sterility Concerns
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Medline Industries Recalls Medical Kits Containing Tego Connectors Due to Seal Defects
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Medline Industries Recalls Meijer Sterile Saline Wound Wash Over Sterility Concerns
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Medline Industries Recalls Nail Kits Due to Potential Sterility Concerns
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Medline Industries Recalls Nail Kits Due to Potential Sterility Issues in Wound Wash
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Medline Industries Recalls Over 10,000 Convenience Kits Due to Sterility Concerns
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Medline Industries Recalls Over 117,000 Convenience Kits Due to Sterility Concerns
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Medline Industries Recalls Over 12,000 Surgical Convenience Kits Due to Sterility Concerns
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Medline Industries Recalls Over 14,000 Dialysis Kits and Trays Due to Tego Connector Seal Defects
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Medline Industries Recalls Over 14 Million Surgical Drapes Due to Sterility Concerns
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Medline Industries Recalls Over 193,000 Surgical Packs Due to Sterilization Concerns
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Medline Industries Recalls Over 27,000 Convenience Kits Due to Sterility Concerns
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Medline Industries Recalls Over 39,000 Convenience Kits Due to Sterility Concerns
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Medline Industries Recalls Over 4,700 Convenience Kits Due to Sterility Concerns
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Medline Industries Recalls Over 70 Million Surgical Gowns Due to Sterility Concerns
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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 PPE Kits Due to Potential Sterility Issues
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Medline Industries Recalls Surgical and Medical Convenience Kits Over Sterility Concerns
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Medline Industries Recalls Surgical Convenience Kits Over Sterility Concerns
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Medline Industries Recalls Tracheostomy Convenience Kits Due to Sterility Concerns
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Medline Industries Recalls Urology Convenience Kits Over Sterility Assurance Concerns
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Medline Recalls Convenience GI Kits Over Potential Sterility Assurance Issues
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Medline Recalls Over 3.5 Million Units of Sterile Saline Wound Wash Due to Sterility Concerns
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Medline Recalls Triple Lumen Insertion Kits Over Sterilization Equipment Calibration Issues
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Medtronic Recalls Octopus Nuvo Tissue Stabilizers Due to Assembly Error
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MIN JIANG FOOD STORE INC Recalls Frozen Fish Balls Due to Undeclared Wheat and Sesame
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MRIMed Inc. Recalls MRI LED Mobile Exam Light Batteries Due to Overheating and Smoke Hazard
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Navitas Organics Recalls Organic Chia Seeds Due to Potential Salmonella Contamination
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Olympus Corporation of the Americas Recalls Inner Sheath Devices Due to Breaking Ceramic Tips
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Olympus Corporation Recalls Cystoscope Outer Sheaths Due to Laser Incompatibility
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Olympus Corporation Recalls Resection Inner Sheaths Due to Ceramic Tip Breakage Risk
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Olympus Corporation Recalls Resection Sheaths Due to Risk of Ceramic Tip Breakage
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Olympus Corporation Recalls Resection Sheaths Due to Risk of Ceramic Tip Breaking
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Olympus Corporation Recalls Thunderbeat Surgical Devices Due to Adverse Event Reports
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Olympus Issues Recall for Inner Sheath Used in Urological Procedures Due to Breaking Ceramic Tips
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Olympus Issues Recall for Resection Sheath Due to Risk of Ceramic Tip Breakage
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Olympus Issues Recall for Resection Sheaths Due to Risk of Ceramic Tip Breakage
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Olympus Recalls High Flow Insufflation Units Due to Overpressure Risk
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Olympus Recalls High Flow Insufflation Units Due to Software-Related Overpressure Risk
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Olympus Recalls High Flow Insufflation Units Over Software-Related Overpressure Risk
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Olympus Recalls Inner Sheath 21 Fr. Model A2660T Over Ceramic Tip Breakage Concerns
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Olympus Recalls Inner Sheath Model A2642 Over Reports of Breaking Ceramic Tips
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Olympus Recalls Inner Sheaths Due to Risk of Ceramic Tip Breakage
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