FDA Recalls, Food, Drug & Medical Device Alerts - Page 11 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 501–550 of 2,262 FDA recalls. Browse by month →
FDA Recalls
Philips Telemetry Monitor 5500 Recall
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FDA Recalls
Zimmer Off-Axis Reamer Guide Recall
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FDA Recalls
Surgify Halo Drill Recall Issued for Burr Breakage Risk
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FDA Recalls
Surgify Halo Drill Recall Issued by FDA
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FDA Recalls
Zimmer Off-Axis Shoulder System Reamer Guide Recall
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FDA Recalls
Acumed Hexalob Screws Recall Due to Breakage Risk
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FDA Recalls
Zimmer Off-Axis Alliance Glenoid Recall
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FDA Recalls
Medline Convenience Kits Recall for Unapproved Design Changes
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FDA Recalls
Medline Convenience Kits Recall for Unapproved Design Changes
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FDA Recalls
Medline Convenience Kits Recall Issued for Unapproved Design Changes
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FDA Recalls high
Abiomed Impella CP Set with SmartAssist Recall
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FDA Recalls
Medline Convenience Kits Recall for Unapproved Design Changes
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FDA Recalls
Surgify Halo Drill Recall Issued by FDA
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FDA Recalls
Surgify Halo Drill Recall Issued for Burr Breakage Risk
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FDA Recalls
Surgify Halo 3.0 mm Drill Recall Issued for Breakage Risk
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FDA Recalls
Surgify Halo Drill Recall Issued by FDA
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FDA Recalls
Medline Convenience Kits Recall for Unapproved Design Changes
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FDA Recalls
Medline Convenience Kits Recall for Unapproved Design Changes
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FDA Recalls
Surgify Halo Drill Recall Issued for Burr Breakage Risk
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FDA Recalls high
Medline Convenience Kits Recall
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FDA Recalls
TMJ Bilateral Implants Recall Issued by TMJ Solutions Inc
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FDA Recalls high
Medline Convenience Kits Recall
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FDA Recalls
Surgify Halo Drill Recall Issued Over Burr Breakage Risk
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FDA Recalls
Surgify Halo Drill Recall Issued for Burr Breakage Risk
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FDA Recalls
Philips Avalon Fetal Monitor Recall Issued
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FDA Recalls
Medtronic Octopus Evolution Tissue Stabilizer Recall
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FDA Recalls
GE Healthcare AW Server 3.2 Recall for Synchronization Issue
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FDA Recalls
Medline Convenience Kits Recall for Unapproved Design Changes
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FDA Recalls
Surgify Halo Drill Recall Due to Burr Breakage Risk
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FDA Recalls
Medline Major Basin Set Kits Recall
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FDA Recalls high
Medline Convenience Kits Recall Issued
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FDA Recalls
Medline Convenience Kits Recall for Unapproved Design Changes
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FDA Recalls
Medline Convenience Kits Recall Due to Design Changes
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FDA Recalls
Medline Convenience Kits Recall for Unapproved Syringe Design
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FDA Recalls
Surgify Halo Drill Recall Issued for Burr Breakage Risk
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FDA Recalls
PFM Medical Multi-Snare Set Recall Issued
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FDA Recalls high
Medline Convenience Kits Recall
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FDA Recalls
Medline Convenience Kits Recall
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FDA Recalls
Surgify Halo Drill Recall for Potential Burr Breakage
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FDA Recalls high
Abiomed Impella Introducer Kit Recall
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FDA Recalls
Zimmer Persona Revision Femoral Distal Augment Recall
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FDA Recalls
Thuvera Laser Console Recall Issued by IPG Medical
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FDA Recalls
Boston Scientific Recalls INTERA 3000 Hepatic Artery Infusion Pump
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FDA Recalls
Medline Convenience Kits Recall Issued
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FDA Recalls
Surgify Halo Recall Issued for Potential Burr Breakage
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FDA Recalls
Octopus 4 Tissue Stabilizer Recall
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FDA Recalls
Da Vinci ASSY PSS SP1098 Recall
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FDA Recalls
Stryker Neurovascular Recalls INZONE DETACHMENT SYSTEM
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FDA Recalls
Surgify Halo Drill Recall Issued for Burr Breakage Risk
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FDA Recalls high
Abiomed Impella Introducer Kit Recall
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