Browse Device Recalls

163 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 163 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 163 FDA device recalls.

Clear
DateProductReasonClassFirm
Jun 22, 2017 AVID TruCustom OBSTETRICAL PACK convenience kits, Item Code: HLDH008-04 Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles t... Class II Avid Medical, Inc.
Jun 22, 2017 AVID TruCustom EXTREMITY PACK convenience kits, Item Code: MADN012-01 and MAD... Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles t... Class II Avid Medical, Inc.
Jun 22, 2017 AVID TruCustom NEURO PK convenience kits, Item Code: LGHM021-08 Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles t... Class II Avid Medical, Inc.
Jun 22, 2017 AVID TruCustom MINOR PROCEDURE 6A convenience kits, Item Code: MADN032-01 Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles t... Class II Avid Medical, Inc.
Jun 22, 2017 AVID TruCustom SHOULDER ARTHROSCOPY convenience kits, Item Code: MADN010-02 Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles t... Class II Avid Medical, Inc.
Jun 22, 2017 AVID TruCustom GENERAL PACK convenience kits, Item Code: LGHM041-06 and LGHM0... Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles t... Class II Avid Medical, Inc.
Jun 22, 2017 AVID TruCustom KNEE ARTHROSCOPY PACK convenience kits, Item Code: MADN011-02 Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles t... Class II Avid Medical, Inc.
Jun 22, 2017 AVID TruCustom DAVINCI PACK convenience kits, Item Code: ADVU037-09 Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles t... Class II Avid Medical, Inc.
Mar 15, 2017 Vacutainer Tubes Vacutainer tubes are intended for clinical laboratory hemat... Avid Medical Inc has received a complaint was received from an end-user indicating the vacutainer... Class II Avid Medical, Inc.
Oct 5, 2015 MAMMOGRAPHY Avid Medical Inc. states a latex-containing Telfa" Non-adherent Dressing 4"x3" (10.2cm x 7.6 em) ... Class II Avid Medical, Inc.
Oct 5, 2015 Convenience Kits, MOHS "OPENING" PROCEDURE TRAY Avid Medical Inc. states a latex-containing Telfa" Non-adherent Dressing 4"x3" (10.2cm x 7.6 em) ... Class II Avid Medical, Inc.
Oct 5, 2015 Convenience Kits, MOHS "OPENING" PROCEDURE TRAY Avid Medical Inc. states a latex-containing Telfa" Non-adherent Dressing 4"x3" (10.2cm x 7.6 em) ... Class II Avid Medical, Inc.
Oct 5, 2015 PEDIATRIC KIDNEY BIOPSY TRAY Avid Medical Inc. states a latex-containing Telfa" Non-adherent Dressing 4"x3" (10.2cm x 7.6 em) ... Class II Avid Medical, 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.