FDA Recalls, Food, Drug & Medical Device Alerts - Page 38 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 1,851–1,900 of 2,262 FDA recalls. Browse by month →
FDA Recalls
Recall of Tops GOLD Stuffed Red Chilli Pickle Due to Potential Adulteration
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FDA Recalls
Recall of CUROSURF Drug by Chiesi USA Due to Sterility Concerns
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FDA Recalls
Recall of Sodium Iodide I-131 Due to Failed Specifications
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FDA Recalls
FDA Issues Recall for Meclizine Hydrochloride Tablets
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FDA Recalls
Recall of Octreotide Acetate Injection by Teva Pharmaceuticals
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FDA Recalls
FDA Recall of Levothyroxine Sodium Tablets Due to Subpotency
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FDA Recalls
Agebox Recalls iKids-Growth Capsules Due to Undeclared Ibutamoren
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FDA Recalls high
Agebox Recalls iKids-Growth Night Formula Due to Undeclared Ibutamoren
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FDA Recalls
Agiliti Health Recalls Adapt Pump Support Surfaces Due to Software Malfunction
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FDA Recalls
Auris Health Recalls MONARCH Bronchoscopy Platform Due to Software Malfunction
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FDA Recalls
AvKARE Issues Voluntary Recall for Amantadine HCl Capsules Due to Dissolution Failure
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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
Baxter Healthcare Recalls Spectrum IQ Infusion Pumps Due to Missing Safety Testing
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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
Edermy LLC Issues Recall for PIE Trolley System Model 2005 Due to Lack of FDA Clearance
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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
Encore Medical, LP Recalls Reverse Shoulder Prosthesis Humeral Socket Inserts Due to Incorrect Labeling
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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
Encore Medical Recalls EMPOWR 3D KNEE Implants Due to Incorrect Labeling
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H & N Group Inc. Recalls Frozen Cooked Shrimp Due to Potential Cesium-137 Contamination
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FDA Recalls
Hitachi Recalls PROBEAT-CR Proton Beam Therapy System Due to Software Anomaly
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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
Integra LifeSciences Recalls MEDIHONEY Calcium Alginate Dressings Due to Potential Sterility Breach
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Integra LifeSciences Recalls MediHoney Gel Due to Potential Sterile Barrier Breach
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Integra LifeSciences Recalls Private Label CVS Wound Care Products Over Sterility Concerns
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FDA Recalls
Intuitive Surgical Recalls Da Vinci 5 Surgical Consoles Due to Software Error
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LEO Pharma Inc. Recalls Adbry Injection Due to Potential Wool Fiber Contamination
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Lotus Mom Corporation Recalls Brass Tope Over Potential Lead Contamination
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FDA Recalls
Lubna Quality Products Inc. Recalls Mung Beans in Texas and Louisiana Due to Pesticide
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Medica Corporation Recalls Capillary Tube Kits Due to Inaccurate Potassium Results
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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 3,561 Medical Convenience Kits Over Sterility Concerns
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Medline Industries Recalls 30,958 Convenience Kits Over Sterility Concerns
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Medline Industries Recalls 4,853 Convenience Kits Over Sterilization Calibration Issues
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Medline Industries Recalls 5,346 Medical Convenience Kits Over Sterility Concerns
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Medline Industries Recalls 7,494 Neuro Convenience Kits Over Sterility Concerns
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Medline Industries Recalls 82,597 Surgical Convenience Kits Over Sterility Concerns
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Medline Industries Recalls 9,051 Convenience Kits Over Sterility Assurance Concerns
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Medline Industries Recalls Admit Kits Due to Potential Sterility Compromise
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FDA Recalls
Medline Industries Recalls Arthroscopy Kits and Trays 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 high
Medline Industries Recalls Burn Packs Over Sterilization Equipment Calibration Issues
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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 Chest/Breast Convenience Kits Due to Sterility Concerns
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FDA Recalls
Medline Industries Recalls Convenience Kits Due to Potential Sterility Assurance Issues
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FDA Recalls
Medline Industries Recalls Convenience Kits Due to Potential Sterility Concerns
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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 Over Potential Sterility Concerns
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FDA Recalls
Medline Industries Recalls Convenience Kits Over Sterility Concerns
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