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Browse Device Recalls

3 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 3 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 3 FDA device recalls.

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DateProductReasonClassFirm
Apr 12, 2017 Savaria SL-1000 Stairlift The electrical controller, combined with motor, causes feedback, damaging a component on the cont... Class II Savaria Concord Lifts, Inc.
Apr 12, 2017 The Savaria Stairfriend is a Residential, commercial, indoor, stair lift for ... Savaria Concord Lifts has decided to initiate a recall of the Stairfriend, because of product def... Class II Savaria Concord Lifts, Inc.
Apr 12, 2017 Omega Incline Platform Lift Savaria Concord Lifts Inc has decided to initiate this recall of its Omega Incline Platform Lift ... Class II Savaria Concord Lifts, 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.