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Vehicle Safety

Vehicle Recalls320,000+ NHTSA safety recalls Browse VehiclesEvery make, model and year Complaints2.1M+ consumer safety complaints TSBs4.7M technical service bulletins VIN LookupDecode any vehicle VIN instantly OBD Codes12,000+ diagnostic trouble codes Fuel EconomyEPA MPG data for all vehicles Safety Ratings11,700+ NHTSA crash test ratings Investigations5,300+ NHTSA defect investigations StatisticsRecall trends & safety analysis Compare VehiclesTwo vehicles side by side

Consumer Safety

Product Safety9,700+ CPSC product recalls Food Safety28,600+ FDA food recalls Pet Safety1.3M FDA animal adverse events Drug Safety17,500+ FDA drug recalls Device Safety38,400+ FDA device recalls Workplace Safety102,900+ OSHA injury reports Brand HistoryRecall lookup by company

Infrastructure

Bridge Safety624,000 bridge inspections Aviation Safety30,000+ NTSB aviation events Dam Safety92,600 dam safety records Water Safety433,000+ public water systems Railroad Safety438,000+ rail crossings Pipeline Safety8,800+ pipeline incidents State DashboardsSafety grades for all 50 states ZIP ReportAny 5-digit ZIP across 9 datasets

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Browse Device Recalls

1,506 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 1,506 FDA medical device recall enforcement actions. Each entry includes the device description, reason for recall, classification (Class I through III based on severity), recalling firm, and distribution details. Use the filters below to search by year, classification, state, or keyword.

Medical Device Recalls

Browse 1,506 FDA device recalls in FL.

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DateProductReasonClassFirm
Jun 16, 2010 Product is labeled in part: "***MEDLINE***Extended PTFE Coated Needle 4.0" (... On 6/16/2010 Unimed Surgical Products, Inc., 10401 Belcher Road, Largo, FL 33777 initiated a reca... Class II Unimed Surgical Products, Inc.
Jun 16, 2010 Product is labeled in part: "***MEDLINE***Standard PTFE Coated Needle 2.75" ... On 6/16/2010 Unimed Surgical Products, Inc., 10401 Belcher Road, Largo, FL 33777 initiated a reca... Class II Unimed Surgical Products, Inc.
Jan 21, 2010 Lockheed Martin Gyrocam Systems ( LMGS) LMGS 15" camera systems. Laser pointe... These camera systems were manufactured by LMGS and found to fail to comply with the FDA laser pe... Class II Lockheed Martin Gyrocam Systems, Inc.
Jun 4, 2009 Apelo Modular Screwdriver labeled in part: "APELO PEDICLE SCREW SYSTEM***Modu... Atlas Spine, Inc. recalled their Apelo Modular Screwdriver, a component of the Apelo Pedicle Scre... Class II Atlas Spine, Inc.
Mar 6, 2009 Altiva / Exactech Spine, Large Set Screw, Catalog Number 28202, Lot Number AS... Incorrect thread form on the screw. Class II Exactech, Inc.
Jul 16, 2008 Various SRI Surgical Disposable Accessory Packs. SRI's Disposable Accessor... Distribution of a product that did not meet specifications. (labeling error) Class II SRI Surgical

Frequently Asked Questions

When a device safety issue is identified, the manufacturer or FDA initiates a recall. The FDA publishes an enforcement report detailing the device, the reason for the recall, and distribution. Healthcare facilities and providers are notified to check their inventory and take corrective action.

All types — from simple devices like blood glucose test strips and surgical gloves to complex devices like pacemakers, defibrillators, insulin pumps, hip implants, and ventilators. Software-driven devices are increasingly common in recalls due to bugs and cybersecurity vulnerabilities.

Use the search and filter tools on this page. Each recall entry includes the device description, model numbers, and distribution details so you can determine if your device is affected. Contact your healthcare provider if you find a match.