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Browse Device Recalls

5 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 5 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 5 FDA device recalls.

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DateProductReasonClassFirm
Feb 4, 2019 Molift 2-Point sling bar, an accessory for Molift Mover 205. Item nos. 143001... The firm has received 7 reports of malfunction for the device in which the hooks have broken off,... Class II Moller Vital
Feb 4, 2019 Molift 2-Point sling bar, an accessory for Molift Mover 180/Air. Item nos. 18... The firm has received 7 reports of malfunction for the device in which the hooks have broken off,... Class II Moller Vital
Jun 24, 2016 Molift Air 205, Molift Air 205 Propulsion, Molift Air IRC, Molift Air 205 IRC... Potential for the bolt on the suspension coupling on the Molift Air to come loose from the housing. Class II Moller Vital
Feb 15, 2013 Molift Smart 150 The leg spreading mechanism will fail to hoist and collapse if assemble incorrectly by the user. Class II Moller Vital
Feb 15, 2013 Molift Smart 150 The leg spreading mechanism will fail to hoist and collapse if assemble incorrectly by the user. Class II Moller Vital

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.