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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

2,560 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 2,560 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 2,560 FDA device recalls in IN.

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DateProductReasonClassFirm
Oct 10, 2010 00789503201 VerSys Femoral Head Provisional 32mm -3.5 00789503202 VerSys Fem... Surgical technique instructions for the Versys and Slotted Provisional Femoral Heads have been en... Class II Zimmer, Inc.
Oct 10, 2010 00780302601 MIS 12/14 Slotted Femoral Head Provisional -3.5X26 00780302602 M... Surgical technique instructions for the Versys and Slotted Provisional Femoral Heads have been en... Class II Zimmer, Inc.
Oct 10, 2010 00780302801 MIS 12/14 Slotted Femoral Head Provisional -3.5X28 00780302802 M... Surgical technique instructions for the Versys and Slotted Provisional Femoral Heads have been en... Class II Zimmer, Inc.
Oct 10, 2010 . 00789502801 VerSys Femoral Head Provisional 28mm -3.5 00789502802 VerSys F... Surgical technique instructions for the Versys and Slotted Provisional Femoral Heads have been en... Class II Zimmer, Inc.
Oct 10, 2010 00780303601 MIS 12/14 Slotted Femoral Head Provisional -3.5X36 00780303602 M... Surgical technique instructions for the Versys and Slotted Provisional Femoral Heads have been en... Class II Zimmer, Inc.
Oct 10, 2010 00780302201 MIS 12/14 Slotted Femoral Head Provisional -2X22 00780302202 MIS... Surgical technique instructions for the Versys and Slotted Provisional Femoral Heads have been en... Class II Zimmer, Inc.
Oct 10, 2010 00780304001 MIS 12/14 Slotted Femoral Head Provisional -3.5X36 00780304002 M... Surgical technique instructions for the Versys and Slotted Provisional Femoral Heads have been en... Class II Zimmer, Inc.
Oct 10, 2010 00780303201 MIS 12/14 Slotted Femoral Head Provisional -3.5X32 00780303202 M... Surgical technique instructions for the Versys and Slotted Provisional Femoral Heads have been en... Class II Zimmer, Inc.
Oct 10, 2010 00789504001 VerSys Femoral Head Provisional 40mm -3.5 00789504002 VerSys Fem... Surgical technique instructions for the Versys and Slotted Provisional Femoral Heads have been en... Class II Zimmer, Inc.
Dec 12, 2006 PT113950 PT HYBRID Glenoid Post Regenerex porous titanium construct Sterile... Biomet is recalling Part Number PT-113950 PT Hybrid Glenoid Post, following an investigation whi... Class II Biomet, Inc.

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.