FDA Recalls, Food, Drug & Medical Device Alerts - Page 45 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 2,201–2,250 of 2,262 FDA recalls. Browse by month →
FDA Recalls
Vantive US Healthcare Recalls Prismaflex ST150 Sets Due to Chamber Dislodgement Risk
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FDA Recalls
Vantive US Healthcare Recalls Prismaflex TPE2000 Sets Due to Component Dislodgement Risk
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FDA Recalls
Ventura Foods LLC Recalls Multiple Peanut Butter Brands Due to Potential Plastic Contamination
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FDA Recalls
Ventura Foods LLC Recalls Poco Pac Peanut Butter and Jelly Packs Over Plastic Contamination
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FDA Recalls
Ventura Foods LLC Recalls Poco Pac Peanut Butter and Strawberry Jam Due to Potential Plastic Contamination
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FDA Recalls high
Venzu Traders LLC Recalls Cinnamon Powder Due to Potential Lead Contamination
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FDA Recalls
Vivoo pH Test Recalled Due to Lack of Marketing Clearance and Risk of Inaccurate Results
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Vortex Surgical Inc. Recalls Convenience Kits Over Potential Sterility Breach
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Olympus Recalls ShockPulse-SE Lithotripsy System Probes Due to Recognition Issues
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FDA Recalls
Advanced Bionics Recalls Sky CI M90 Sound Processors Due to Labeling Error
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FDA Recalls
Olympus Recalls ShockPulse-SE Lithotripsy Systems Due to Mis-wired Components
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FDA Recalls
Vascutek, Ltd. Recalls Gelsoft Plus and Gelweave Vascular Devices Due to Incorrect Shelf Life Labeling
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FDA Recalls
Diagnostica Stago Recalls STA Liatest Free Protein S Kits for Inaccurate Test Results
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FDA Recalls
Olympus Recalls ShockPulse-SE Lithotripsy System Reusable Probes Due to Recognition Issues
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FDA Recalls
Datascope Corp. Recalls CS100 IABP Devices Due to Battery Specification Updates
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FDA Recalls
Siemens Healthcare Diagnostics Recalls Atellica CH Urine Albumin Test Kits Due to Inaccurate Results
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FDA Recalls
Datascope Corp. Recalls CS300 IABP Devices to Update Battery Specifications
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FDA Recalls high
GE Healthcare Recalls Centricity Universal Viewer Zero Footprint Client Due to Patient Data Mismatch
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Roche Diagnostics Recalls cobas pro Integrated Solutions Due to Software Defect
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FDA Recalls
ESAOTE S.P.A. Recalls Endocavity Ultrasonic Probes Due to Potential Liquid Leakage
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FDA Recalls
Aesculap Inc. Recalls MINOP Trocar Devices Due to Incorrect Shaft Length
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FDA Recalls high
Staar Surgical AG Recalls EVO+ Visian Toric Implantable Collamer Lenses Due to Labeling Error
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FDA Recalls high
Abiomed Recalls Impella RP Heart Pumps Over Sensor Malfunction Risks
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FDA Recalls
Olympus Recalls ShockPulse-SE Lithotripsy System Generators Over Recognition Failure
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FDA Recalls high
Abiomed, Inc. Issues Recall for Impella RP with SmartAssist Over Sensor Malfunction
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FDA Recalls
Olympus Recalls Single Use Biopsy Valves Due to Rubber Fragment Detachment Risk
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FDA Recalls high
Abiomed Recalls Impella RP Flex with SmartAssist Heart Pumps Due to Sensor Malfunction
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Olympus Recalls Single Use Biopsy Valves Due to Potential Rubber Fragment Detachment
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FDA Recalls
Bader Enterprises, Inc. Recalls Premium Food Bubble Gum Over Undeclared Colors
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FDA Recalls
Bader Enterprises Recalls Premium Food Jordan Almonds Over Undeclared Wheat and Colors
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FDA Recalls
Italianway Import, Inc. Recalls Vergani 1944 Milano Gluten-Free Pandoro Due to Potential Teflon Contamination
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FDA Recalls high
Juniper Granola, LLC Recalls Junebar Snack Bars Due to Undeclared Milk and Soy
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FDA Recalls
Tippy Toes Apple Pear Banana Baby Food Recalled Over Patulin Contamination Concerns
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FDA Recalls high
Juniper Granola Recalls Junebar Chocolate Cherry Snack Bars Due to Undeclared Milk and Soy
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SILINTAN 25/pills Recalled Nationwide Due to Undeclared Meloxicam
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Acme United Corporation Recalls Children's Healthcare of Atlanta Hand Sanitizing Wipes
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FDA Recalls
Acme United Corporation Recalls BZK Antiseptic Towelettes Due to Manufacturing Deviations
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FDA Recalls
ACME UNITED CORPORATION Recalls WP WipesPlus Hand Sanitizing Wipes Due to Manufacturing Deviations
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FDA Recalls
Acme United Corporation Recalls Green Guard Antiseptic Wipes Due to Manufacturing Deviations
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FDA Recalls
Radnostix Recalls Sodium Iodide I-131 Therapeutic Oral Solution Due to Particulate Matter
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FDA Recalls
Cipla USA Inc. Issues Nationwide Recall for Nilotinib Capsules Due to Appearance Defects
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FDA Recalls
Harbin Jixianglong Biotech Co. Issues Nationwide Recall of Semaglutide Over Manufacturing Deviations
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FDA Recalls
Acme United Corporation Recalls Dukal BZK Antiseptic Towelettes Due to CGMP Deviations
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FDA Recalls
Medi-First Antiseptic Wipes Recalled Nationwide Due to Manufacturing Deviations
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FDA Recalls
ACME UNITED CORPORATION Recalls Max Packaging Antibacterial Towelettes Due to CGMP Deviations
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FDA Recalls
ACME UNITED CORPORATION Recalls Antimicrobial Alcohol Hand Wipes Due to CGMP Deviations
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FDA Recalls
Teva Pharmaceuticals Recalls Metoprolol Succinate Extended-Release Tablets Due to Dissolution Failure
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FDA Recalls
ACME UNITED CORPORATION Recalls Dynarex Obstetrical Towelettes Cleanser Due to CGMP Deviations
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FDA Recalls
HTO Nevada Inc. Issues Recall for Maximum Zone 1 Lidocaine Cream Due to Stability Concerns
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FDA Recalls
Acme United Corporation Recalls First Aid Only Hand Sanitizing Wipes Due to Manufacturing Deviations
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