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Browse Device Recalls

5 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 5 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 5 FDA device recalls.

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DateProductReasonClassFirm
Nov 29, 2016 symmetry surgical ULTRA(R) Sterrad container, REF numbers: C131310-SP, C1313... Sealant on the base trim of sterilizer container may be deteriorated or absent which could provid... Class II Symmetry Surgical, Inc.
Nov 29, 2016 symmetry surgical ULTRA(R) Gravity container, REF numbers: C131310-G, C13134... Sealant on the base trim of sterilizer container may be deteriorated or absent which could provid... Class II Symmetry Surgical, Inc.
Nov 29, 2016 symmetry surgical ULTRA(R) Steam container, REF numbers: C131310, C13134, C1... Sealant on the base trim of sterilizer container may be deteriorated or absent which could provid... Class II Symmetry Surgical, Inc.
Jun 16, 2015 SYMMETRY SURGICAL DISPOSABLE TOWEL CLAMP, REF 19-4137, STERILE EO, Rx only. ... Lack of sterility assurance. Class II Symmetry Surgical, Inc.
Dec 5, 2013 Symmetry and CODMAN brands, QUAD-LOCK Sterilization Container. Sterilization ... The Quad-Lock Sterilization Container System may not maintain an effective sterile barrier. Class II Symmetry Medical/SSI

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.