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Browse Device Recalls

8 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 8 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 8 FDA device recalls.

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DateProductReasonClassFirm
Jul 14, 2025 Corin Operating Tables Model Numbers: (1) 770001A0, (2) 770001A2, (3) 770001... Under certain conditions, such as the simultaneous use of the operating table with other medical ... Class II MAQUET GMBH
Jan 7, 2016 Maquet Getinge Group 1180.19XO Extension Device. Manufacturer MAQUET GmbH, ... MAQUET Medical Systems USA is initiating a field action for correction of the MAQUET Extension De... Class II Maquet Cardiovascular Us Sales, Llc
Aug 17, 2015 Maquet Getinge Group, Adjustable Positioning Elements (1007.28A0) Manufacture... Two serious thromboembolic events were reported involving the Adjustable Positioning Elements (Pa... Class II Maquet Cardiovascular Us Sales, Llc
Aug 17, 2015 Maquet Getinge Group, Universal Frame for Positioning Patients (1007.24XX) Ma... Two serious thromboembolic events were reported involving the Adjustable Positioning Elements (Pa... Class II Maquet Cardiovascular Us Sales, Llc
Jun 10, 2015 Magnus Hybrid OR Table Column (1180.01B2) used in conjunction with Siemens Ar... There is a potential issue that could result to collision between the C-arm of the angiography sy... Class II Maquet Cardiovascular Us Sales, Llc
Aug 21, 2014 TEGRIS System manufactured by MAQUET GMBH in Germany The Maquet Tegris OR In... The wrong movement results on the MAGNUS OR table. The button commands on the TEGRIS touchscreen ... Class II Maquet Medical Systems USA
Aug 19, 2013 TEGRIS system Four labels of the Tegris System include: Emergency butt... MAQUET has identified a potential issue that might occur because of the lack of an emergency stop... Class II Maquet Cardiovascular Us Sales, Llc
Nov 2, 2012 Maquet Yuno Extension Table Device Maquet GmbH & Co. KG Kehler Strabe 31 B... There is a potential issue with the screw tension of the extension device 1433.62A1 used with the... Class II Maquet 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.