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Browse Device Recalls

4 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 4 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 4 FDA device recalls.

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DateProductReasonClassFirm
Jul 12, 2015 Etac Relax wall mounted shower seat The Etac Relax is a wall mounted shower ... The recalling firm has received reports of a malfunction of the Relax wall mounted shower seat wh... Class II Etac Supply Center Ab
Jun 15, 2015 Etac Supporter toilet armrest Etac Supporter toilet armrests are foldable an... The Supporter toilet armrest has two Fast Nuts fixing the product to the toilet porcelain. The fi... Class II Etac Supply Center Ab
May 23, 2013 Swift Mobil shower chair, Swift Mobil 160 shower chair, and Swift Mobil Tilt ... Etac is voluntarily conducting a field correction of the Etac Swift Mobil shower chair. If the Sw... Class II Etac Supply Center Ab
Apr 6, 2012 Etac¿ Ono Walker, Etac¿ Avant Walker, and Etac¿ Salsa Walker. These produ... The recall has been initiated because there is the potential that users may fall and become injur... Class II Etac Supply Center Ab

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.