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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
Mar 22, 2021 Normand Remisol Advance Data Manager is a software device that interfaces bet... Instructions For Use for software versions 1.5 to 1.9 did not provide sufficient instructions reg... Class II Normand-Info S.A.S.U.
Apr 30, 2020 Remisol Advance running Software Version 1.12 The Normand Info Remisol Adv... Results from repeated run for WBC (White Bloodcell Count), UWBC (Urine Whit Bloodcell Count) and ... Class II Normand-Info S.A.S.U.
Aug 15, 2019 Remisol Advance running on hardware with Windows XP, Windows 7, Windows Serve... A patch was released for a critical remote code execution vulnerability in remote desktop service... Class II Normand-Info S.A.S.U.

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.