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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

1,006 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 1,006 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 1,006 FDA device recalls.

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DateProductReasonClassFirm
Oct 19, 2007 GEHC OEC 8800 Mobile Fluoroscopic X-ray System, GE Healthcare, Surgery, Salt ... X-ray units did not meet manufacturer's specification for linearity. Class II GE OEC Medical Systems, Inc
Nov 8, 2006 The Axcess Cranial Screw (sometimes referred to as the Axcess Cranial Pin) is... GE Healthcare is aware of a few instances where the Axcess Cranial Screw has broken during insert... Class II GE OEC Medical Systems, Inc
Oct 11, 2006 OEC InstaTrak 3500, picture archiving and communications system intended as a... GE Healthcare had recalled certain OEC InstaTrak 3500 Carts due to the potential for the cart to ... Class II GE OEC Medical Systems, Inc
Sep 15, 2006 InstaTrak with Multiple Dataset Navigation, 892.2050 System, Image Processing... Please be aware that this is not a new recall. The firm has taken action; but, due to administra... Class I GE OEC Medical Systems, Inc
May 31, 2006 GE Healthcare Definium 8000 Digital Radiographic Systems : GE Healthcare, 3... An incident was reported that an operator's finger was pinched between the fixed roller and the g... Class II General Electric Med Systems LLC
May 31, 2006 GE Healthcare Revolution XR/d; GE Healthcare, 3000 North Grandview , Waukesha... An incident was reported that an operator's finger was pinched between the fixed roller and the g... Class II General Electric Med Systems LLC

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.