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Browse Device Recalls

12 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 12 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 12 FDA device recalls.

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DateProductReasonClassFirm
Apr 20, 2012 Grafton DBM Orthoblend Small Defect Multiple Sizes Grafton is a human bon... Multiple lots of GRAFTON ¿ and XPANSE ¿, which are used for bone grafting procedures are being r... Class II Osteotech Inc
Apr 20, 2012 Grafton DBM A-Flex Multiple Sizes Grafton is a human bone allograft produ... Multiple lots of GRAFTON ¿ and XPANSE ¿, which are used for bone grafting procedures are being r... Class II Osteotech Inc
Apr 20, 2012 Optimum Expanse R Grafton is a human bone allograft product containing dem... Multiple lots of GRAFTON ¿ and XPANSE ¿, which are used for bone grafting procedures are being r... Class II Osteotech Inc
Apr 20, 2012 Grafton DBM Gel Multiple Sizes Grafton is a human bone allograft product ... Multiple lots of GRAFTON ¿ and XPANSE ¿, which are used for bone grafting procedures are being r... Class II Osteotech Inc
Apr 20, 2012 Grafton DBM Flex Multiple Sizes Grafton is a human bone allograft product... Multiple lots of GRAFTON ¿ and XPANSE ¿, which are used for bone grafting procedures are being r... Class II Osteotech Inc
Apr 20, 2012 Optimum Expanse S Multiple sizes Grafton is a human bone allograft produc... Multiple lots of GRAFTON ¿ and XPANSE ¿, which are used for bone grafting procedures are being r... Class II Osteotech Inc
Apr 20, 2012 Grafton DBM Orthoblend Large Defect Multiple Sizes Grafton is a human bo... Multiple lots of GRAFTON ¿ and XPANSE ¿, which are used for bone grafting procedures are being r... Class II Osteotech Inc
Apr 20, 2012 Grafton DBM Matrix PLF Multiple Sizes Grafton is a human bone allograft p... Multiple lots of GRAFTON ¿ and XPANSE ¿, which are used for bone grafting procedures are being r... Class II Osteotech Inc
Apr 20, 2012 Grafton DBM Crunch Multiple Sizes Grafton is a human bone allograft produ... Multiple lots of GRAFTON ¿ and XPANSE ¿, which are used for bone grafting procedures are being r... Class II Osteotech Inc
Apr 20, 2012 Grafton DBM Matrix Strips Multiple Sizes Grafton is a human bone allograf... Multiple lots of GRAFTON ¿ and XPANSE ¿, which are used for bone grafting procedures are being r... Class II Osteotech Inc
Apr 20, 2012 Grafton DBM Putty Multiple Sizes Grafton is a human bone allograft produc... Multiple lots of GRAFTON ¿ and XPANSE ¿, which are used for bone grafting procedures are being r... Class II Osteotech Inc
Apr 20, 2012 Grafton DBM Orthoblend Large Defect Multiple Sizes Grafton is a human bo... Multiple lots of GRAFTON ¿ and XPANSE ¿, which are used for bone grafting procedures are being r... Class II Osteotech 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.