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Browse Device Recalls

8 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 8 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 8 FDA device recalls.

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DateProductReasonClassFirm
May 22, 2017 DIASTAT(R) ANA (anti-Nuclear antibody) EURO DIAGNOSTICA, The DIASTAT(R) anti-... FANA200 kit lot TS 3577 was re-worked due to shortened shelf-life. The alert sticker on the kit b... Class III Euro Diagnostica AB
Feb 14, 2017 Euro Diagnostica DIASTAT ANA (anti-nuclear antibody) ELISA DIASTAT ANA (an... Euro Diagnostica has identified a deviation in one of the components of the DIASTAT ANA (FANA200)... Class II Euro Diagnostica AB
Oct 21, 2016 is a quantitative/qualitative enzyme-linked immunosorbent assay (ELISA) for t... Incorrectly labeled Manufactured by DiaSorin, The correct term should be Distributed by DiaSorin. Class III Euro Diagnostica AB
Oct 21, 2016 is a qualitative indirect enzyme immunoassay enzyme-linked immunosorbent assa... Incorrectly labeled Manufactured by DiaSorin, The correct term should be Distributed by DiaSorin. Class III Euro Diagnostica AB
Oct 21, 2016 is a quantitative/qualitative enzyme-linked immunosorbent assay (ELISA) for t... Incorrectly labeled Manufactured by DiaSorin, The correct term should be Distributed by DiaSorin. Class III Euro Diagnostica AB
Oct 21, 2016 is a quantitative/qualitative enzyme-linked immunosorbent assay (ELISA) for t... Incorrectly labeled Manufactured by DiaSorin, The correct term should be Distributed by DiaSorin. Class III Euro Diagnostica AB
Feb 14, 2016 Immunoscan CCPlus test kit is an enzyme-linked immunosorbent assay (ELISA) fo... Decreasing performance overtime. Class II Euro Diagnostica AB
Oct 15, 2015 DIASTAT anti-Nuclear antibody (ANA) / DIASTAT ANA ELISA. Catalog Number: FANA... Complaint investigation concluded that although product quality requirements stated in the instr... Class II Euro Diagnostica AB

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.