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Browse Device Recalls

13 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 13 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 13 FDA device recalls.

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DateProductReasonClassFirm
Oct 24, 2012 Superstat Modified Collagen Hemostatic Sponge.115mmx115mm Pledget, 1.5%, Part... The recall was initiated because Superstat Corporation has confirmed that no documentation are av... Class II Superstat Corp
Oct 24, 2012 Superstat Modified Collagen Hemostatic Sponge, 85mm x 85mm Pledget, 3.0%, Par... The recall was initiated because Superstat Corporation has confirmed that no documentation are av... Class II Superstat Corp
Oct 24, 2012 Superstat Modified Collagen Hemostatic Sponge, 32mm Disc, 1.5%, Part# 9120-15... The recall was initiated because Superstat Corporation has confirmed that no documentation are av... Class II Superstat Corp
Oct 24, 2012 Superstat Modified Collagen Hemostatic Sponge, 7.5mm x 19mm Cone, 3.0%, Part#... The recall was initiated because Superstat Corporation has confirmed that no documentation are av... Class II Superstat Corp
Oct 24, 2012 Superstat Modified Collagen Hemostatic Sponge, 115mm x 115mm Pledget, 3.0%, P... The recall was initiated because Superstat Corporation has confirmed that no documentation are av... Class II Superstat Corp
Oct 24, 2012 Superstat Modified Collagen Hemostatic Sponge, 2x2 Pledget, 3.0%, Part# 9106-... The recall was initiated because Superstat Corporation has confirmed that no documentation are av... Class II Superstat Corp
Oct 24, 2012 Superstat Modified Collagen Hemostatic Sponge, 50mm Disc, 3.0%, Part# 9200-30... The recall was initiated because Superstat Corporation has confirmed that no documentation are av... Class II Superstat Corp
Oct 24, 2012 Superstat Modified Collagen Hemostatic Sponge, 50mm Disc, 1.5%, Part# 9200-15... The recall was initiated because Superstat Corporation has confirmed that no documentation are av... Class II Superstat Corp
Oct 24, 2012 Superstat Modified Collagen Hemostatic Sponge, 50mm Disc, 3.0%, Part# 9200-30... The recall was initiated because Superstat Corporation has confirmed that no documentation are av... Class II Superstat Corp
Oct 24, 2012 Superstat Modified Collagen Hemostatic Sponge, 2x2 Pledget, 1.5%, Part# 9105-... The recall was initiated because Superstat Corporation has confirmed that no documentation are av... Class II Superstat Corp
Oct 24, 2012 Superstat Modified Collagen Hemostatic Sponge, 85mm x 85mm Pledget, 1.5%, Par... The recall was initiated because Superstat Corporation has confirmed that no documentation are av... Class II Superstat Corp
Oct 24, 2012 Superstat Modified Collagen Hemostatic Sponge, 4x4 Pledget, 3.0%, Part# 9102-... The recall was initiated because Superstat Corporation has confirmed that no documentation are av... Class II Superstat Corp
Oct 24, 2012 Superstat Modified Collagen Hemostatic Sponge, 32mm Disc, 3.0%, Part# 9100-30... The recall was initiated because Superstat Corporation has confirmed that no documentation are av... Class II Superstat Corp

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.