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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
Nov 12, 2015 ORTHO SPEC GRP CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-075 Post-Op... Knee brace could fail to maintain the locked position and a loss of balance or undesired flexion... Class II Corflex
Nov 12, 2015 HAILEY ORTHO CONTENDER POST-OP-KNEE BRACE Model : 75-7500-038 Post-Operativ... Knee brace could fail to maintain the locked position and a loss of balance or undesired flexion... Class II Corflex
Nov 12, 2015 CT ORTHO CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-011 Post-Opera... Knee brace could fail to maintain the locked position and a loss of balance or undesired flexion... Class II Corflex
Nov 12, 2015 ADV ORTHO CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-231 Post-Operati... Knee brace could fail to maintain the locked position and a loss of balance or undesired flexion... Class II Corflex
Nov 12, 2015 Corflex Contender Post-Op Knee Brace Lite Model: 75-7500-000 Post-Operative... Knee brace could fail to maintain the locked position and a loss of balance or undesired flexion... Class II Corflex
Nov 12, 2015 BRIELLE ORTHO CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-087 Post-O... Knee brace could fail to maintain the locked position and a loss of balance or undesired flexion... Class II Corflex
Nov 12, 2015 CONTENDER POST-OP-KNEE BRACE FULL FOAM Model: 75-7550-000 Post-Operative Kn... Knee brace could fail to maintain the locked position and a loss of balance or undesired flexion... Class II Corflex

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.