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Browse Device Recalls

7 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 7 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 7 FDA device recalls.

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DateProductReasonClassFirm
Oct 30, 2013 Medcare Products Max-500 Stand-N-Weigh, Total Support, patient stand, model #... The lift might fail with the labeled 500-lb. load rating. Class II Ergosafe Products LLC DBA Prism Medical Service...
Oct 30, 2013 Medcare Products Max-500 Stand, Total Support, patient stand, model #400006. ... The lift might fail with the labeled 500-lb. load rating. Class II Ergosafe Products LLC DBA Prism Medical Service...
May 23, 2013 BC Hammock Mesh Sling (Junior), product number, 537005. Product Usage: T... The product does not meet the firm's size standards, the product was produced in the incorrect size. Class II Prism Medical Services USA
May 23, 2013 BC Hammock Mesh Sling (Medium), product number, 537005. Product Usage: U... The product does not meet the firm's size standards, the product was produced in the incorrect size. Class II Prism Medical Services USA
May 23, 2013 BC Hammock Mesh Sling (Large), product number, 537030. Product Usage: The... The product does not meet the firm's size standards, the product was produced in the incorrect size. Class II Prism Medical Services USA
May 23, 2013 BC Hammock Mesh Sling (Small), product number, 537010. Product Usage: Th... The product does not meet the firm's size standards, the product was produced in the incorrect size. Class II Prism Medical Services USA
Jan 27, 2013 Prism Medical C-Series Carry Bar, Class I, model number 360755. The inten... The firm replaced the recalled carry bar with a plastic insert with a carry bar with a metal inse... Class II Prism Medical Services USA

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.