FDA Recalls, Food, Drug & Medical Device Alerts - Page 25 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 1,201–1,250 of 1,348 FDA recalls. Browse by month →
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Asteria Health Issues Nationwide Recall of Estradiol Sterile Pellets Due to Metal Contamination Concerns
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Asteria Health Issues Nationwide Recall of Testosterone Sterile Pellets Due to Metal Particulates
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American Health Packaging Recalls Oxycodone Hydrochloride Tablets Due to Defective Blister Seals
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Fresenius Kabi Compounding Recalls Ketamine HCl Injection Over Sterility Concerns
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Fresenius Kabi Compounding, LLC Recalls Thiamine HCl Injection Due to Lack of Sterility Assurance
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Pro Numb Tattoo Numbing Spray Recalled Due to Manufacturing Deviations
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Asteria Health Recalls Testosterone Sterile Pellets Due to Potential Metal Particulate Matter
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Changchun Wancheng Bio-Electron Recalls Vivoo Vaginal pH Tests Due to Lack of Marketing Clearance
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Vortex Surgical Recalls Lindsell Sutured IOL Markers Over Sterility Concerns
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Changchun Wancheng Bio-Electron Recalls Menopause Test Cassettes Over Regulatory Concerns
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Intuitive Surgical Recalls da Vinci X, Xi, and 5 Surgical Systems Due to Software Error
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Fujirebio Diagnostics Recalls Lumipulse G pTau 217 Plasma Immunoreaction Cartridges Due to Inaccurate Results
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ETAC A/S Recalls Molift Mover 300 Mobile Hoists Due to Structural Component Failure
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Wilson-Cook Medical Inc. Recalls Nasal Jejunal Feeding Tubes Due to Missing Components
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Encore Medical Recalls EMPOWR Acetabular System Liners Due to Packaging Discrepancy
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Vortex Surgical Recalls Rumex Disposable Diamond Dusted ILM Elevator Over Sterility Concerns
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Siemens Medical Solutions Recalls NAEOTOM Alpha.Prime Software Applications Over Lack of FDA Clearance
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ETAC A/S Recalls Molift 2-Point Sling Bars Due to Structural Bolt Failure Risk
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Vortex Surgical Recalls Volk Single Use Vitrectomy Lenses Due to Potential Sterility Breach
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Maquet Cardiopulmonary Gmbh Recalls Bubble Sensors Over Cable Durability Concerns
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Changchun Wancheng Bio-Electron Recalls LH One Step Ovulation Test Devices Over Lack of FDA Clearance
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Boston Scientific Recalls AXIOS Stent and Delivery Systems Over Deployment Failures
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Boston Scientific Recalls HOT AXIOS Stent Systems Due to Deployment and Expansion Issues
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Olympus Recalls Single Use Sphincterotome V Due to Potential Performance Failure
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Fujirebio Diagnostics Recalls Lumipulse G Beta-Amyloid 1-42-N Plasma Calibrators Due to Inaccurate Test Results
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Vortex Surgical Inc. Recalls Disposable Forceps and Cannulas Due to Potential Sterility Breach
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Beckman Coulter Recalls CellMek SPS Sample Preparation System Due to Software Error
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Vortex Surgical Recalls 25GA Subretinal Injection Cannula Due to Potential Sterility Breach
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Changchun Wancheng Bio-Electron Recalls Vivoo Sodium, Vitamin C, and Hydration Tests Due to Marketing Violations
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Vivoo pH Test Recalled Due to Lack of Marketing Clearance and Risk of Inaccurate Results
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Olympus Recalls Disposable Triple Lumen Sphincterotome Due to Potential Deformation and Performance Loss
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Changchun Wancheng Bio-Electron Recalls 32,500 Test Strips Over Marketing and Accuracy Concerns
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Vortex Surgical Inc. Recalls Tecfen Retractable Membrane Polisher Due to Sterility Concerns
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Siemens Medical Solutions Recalls NAEOTOM Alpha Software Applications Over Missing FDA Clearance
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Tornier, Inc. Recalls Reversed Peripheral Screws Due to Labeling Error
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Fujirebio Diagnostics Recalls Lumipulse G β-Amyloid 1-42-N Plasma Test Cartridges for Inaccurate Results
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Vortex Surgical Recalls 25GA I.D.D. Internal Delivery Devices Over Sterility Risks
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Changchun Wancheng Bio-Electron Recalls S. Typhi/Para Typhi A Antigen Test Strips Over Marketing Concerns
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Medtronic Recalls MiniMed 780G Insulin Pumps Due to Software Error Suspending Insulin Delivery
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Vortex Surgical Inc. Recalls Oertli Laser Probes Due to Potential Sterility Breach
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Fujirebio Diagnostics Recalls Lumipulse β-Amyloid Plasma Controls Over Inaccurate Alzheimer's Test Results
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Fujirebio Diagnostics Recalls Lumipulse G pTau217/B-Amyloid 1-42 Plasma Ratio Test Due to Inaccurate Results
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Olympus Recalls Single Use Electrosurgical Knife KD-645 Over Tip Breakage Concerns
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Vantive US Healthcare Recalls Prismaflex ST150 Sets Due to Chamber Dislodgement Risk
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Olympus Recalls Single Use Electrosurgical Knife KD-640L Due to Tip Breakage Risk
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Boston Scientific Recalls AXIOS Stent and Delivery System Over Deployment Failures
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Siemens Medical Solutions Recalls SOMATOM X.ceed Software Applications Over Lack of FDA Clearance
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Changchun Wancheng Bio-Electron Recalls Over 91,000 UTI and Urinalysis Test Strips Due to Inaccuracy Risk
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Encore Medical Recalls EMPOWR 3D Knee Tibial Inserts Over Packaging Errors
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Siemens Medical Solutions Recalls NAEOTOM Alpha.Pro Software Applications Due to Lack of FDA Clearance
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