Browse Device Recalls

4 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 4 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 4 FDA device recalls.

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DateProductReasonClassFirm
Mar 30, 2022 HydroMARK Breast Biopsy Marker, Model No. 4010-05-08-T4 Small patient labels do not match the primary device label. The primary device label accurately i... Class II Devicor Medical Products Inc
Sep 7, 2020 Neoprobe GDS Control Unit, Model Number NPCU3 It was discovered during a documentation review that China has the software version as v5.01 appr... Class III Devicor Medical Products Inc
Feb 28, 2017 Mammotome Revolve Dual Vacuum Assist Biopsy System The device is used to s... The device did not have Revolve Stereo Probe labeling, no product code indicating the size and le... Class II Devicor Medical Products Inc
May 19, 2016 Mammotome Revolve Dual Vacuum Assist Biopsy System Model number: MST1009 & MS... A 10 Gauge needle, 9cm long was shipped in an 8 Gauge needle, 15 cm package. Class II Devicor Medical Products 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.