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Browse Device Recalls

6 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 6 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 6 FDA device recalls.

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DateProductReasonClassFirm
Feb 3, 2023 Med-Riser MR600 Patient Lift Risk of boom pivot failing due to the nut securing the boom becoming loose and the bolt to be uns... Class II Med-Mizer, Inc.
Feb 3, 2023 Sit to Stand STS500 Patient Lift Risk of boom pivot failing due to the nut securing the boom becoming loose and the bolt to be uns... Class II Med-Mizer, Inc.
Jul 25, 2018 PR1000 Pivot Rehab Bed AC powered adjustable bed. Under certain conditions, when pivoting bed to the extreme left there are situations where the wi... Class II Med-Mizer, Inc.
Apr 18, 2014 RetractaBed , Clinical Contour, Med - Mizer Inc..... Model SS 799, 120 V, ..... All configurations of the SS Retractabed, Clinical Contour, made prior to June 7 2008 may have ... Class II Med-Mizer, Inc.
Apr 18, 2014 RetractaBed , Clinical Contour, Med - Mizer Inc..... Model SS 801, 802, 803,... All configurations of the SS Retractabed, Clinical Contour, made prior to June 7, 2008 may have... Class II Med-Mizer, Inc.
Apr 18, 2014 RetractaBed , Clinical Contour, Med - Mizer Inc..... Model SS 762 ( 76 " bed... All configurations of the SS Retractabed, Clinical Contour, made prior to June 7 2008 may have ... Class II Med-Mizer, 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.