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Browse Device Recalls

334 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 334 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 334 FDA device recalls.

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DateProductReasonClassFirm
Apr 16, 2015 Major Kit, Sterile-.Kits containing the Devon Light Glove Catalog Number:D... Devon Light Gloves contain splits or holes compromising the sterility Class II Covidien LLC
Apr 16, 2015 Augmentation Kit , Sterile-.Kits containing the Devon Light Glove Catalog Nu... Devon Light Gloves contain splits or holes compromising the sterility Class II Covidien LLC
Apr 16, 2015 Minor Surgical Kits, Sterile-Kits containing the Devon Light Glove Catalog N... Devon Light Gloves contain splits or holes compromising the sterility Class II Covidien LLC
Apr 16, 2015 Double Basin Kit ,Sterile-Kits containing the Devon Light Glove Catalog Numb... Devon Light Gloves contain splits or holes compromising the sterility Class II Covidien LLC
Apr 16, 2015 Non Sterile Subassembly: Catalog Number/Description: SA1008 NONSTERILE SUB... Devon Light Gloves contain splits or holes compromising the sterility Class II Covidien LLC
Apr 16, 2015 Covidien Devon Light Gloves, Sterile-Single Units A disposable, sterile, si... Devon Light Gloves contain splits or holes compromising the sterility Class II Covidien LLC
Apr 16, 2015 Single Basin Kits, Sterile-.Kits containing the Devon Light Glove Catalog ... Devon Light Gloves contain splits or holes compromising the sterility Class II Covidien LLC
Apr 16, 2015 ASC (Breast) Kit, Sterile-Kits containing the Devon Light Glove Catalog Nu... Devon Light Gloves contain splits or holes compromising the sterility Class II Covidien LLC
Oct 1, 2014 Covidien Puritan Bennett 980 Ventilator, Rx ONLY, Made in Ireland., Covidien ... Covidien is recalling certain Puritan Bennett 980 Ventilator Systems due to a blacklight inverter... Class I Nellcor Puritan Bennett Inc. (dba Covidien LP)
Sep 18, 2014 Covidien Kendall Adult Multi-Function Defibrillation Electrodes Part Number:... Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not Compatible for use with Phi... Class I Covidien LLC
Sep 18, 2014 Philips HEARTSTART Multifunction Electrode Pads Part Number: M3718A Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not Compatible for use with Phi... Class I Covidien LLC
Sep 18, 2014 MediChoice¿ Multifunction Electrode Part Number: MC171 OH Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not Compatible for use with Phi... Class I Covidien LLC
Sep 18, 2014 Covidien Kendall 1710H Multi-Function Defibrillation Electrodes Part Number:... Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not Compatible for use with Phi... Class I Covidien LLC
Sep 18, 2014 Covidien Medi-Trace Cadence and Kendall Adult Multi-Function Defibrillation E... Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not Compatible for use with Phi... Class I Covidien LLC
Sep 18, 2014 Coviden Medi-Trace Cadence Adult Multi-Function Defibrillation Electrodes, Pr... Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not Compatible for use with Phi... Class I Covidien LLC
May 8, 2014 Devon Supine, Lithotomy and Trendelenburg Positioning Kit; Product Code: 3115... Straps may separate from the foam pad. Class II Covidien LLC
Aug 16, 2013 Monoject 10 Units/mL Heparin Lock Flush, 12 mL Syringe with 10 mL Fill Produ... Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin Class II Covidien LLC
Aug 16, 2013 Monoject 0.9% Sodium Chloride Flush Syringe, 12 mL Syringe with 5 mL Fill Pr... Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin Class II Covidien LLC
Aug 16, 2013 Monoject 0.9% Sodium Chloride Flush Syringe, 12 mL Syringe with 3 mL Fill Pr... Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin Class II Covidien LLC
Aug 16, 2013 Monoject 100 Units/mL Heparin Lock Flush, 12 mL Syringe with 10 mL Fill Prod... Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin Class II Covidien LLC
Aug 16, 2013 Monoject 10 Units/mL Heparin Lock Flush, 12 mL Syringe with 5 mL Fill Produc... Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin Class II Covidien LLC
Aug 16, 2013 Monoject 100 Units/mL Heparin Lock Flush, 12 mL Syringe with 3 mL Fill Produ... Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin Class II Covidien LLC
Aug 16, 2013 Monoject 100 Units/mL Heparin Lock Flush, 12 mL Syringe with 5 mL Fill Produ... Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin Class II Covidien LLC
Aug 16, 2013 Monoject 0.9% Sodium Chloride Flush Syringe, 12 mL Syringe with 10 mL Fill P... Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin Class II Covidien LLC
Aug 16, 2013 Monoject 10 Units/mL Heparin Lock Flush, 12 mL Syringe with 3 mL Fill Produc... Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin Class II Covidien LLC
Apr 12, 2013 Curity Staple Remover Kit; Product Code: 66701. Staple Remover Kit. On March 26, 2013 Covidien received a recall notice from one of their suppliers CareFusion. Care... Class III Covidien LLC
Apr 12, 2013 Curity I.V. Start Kit, Product ID: 80530 and Curity I.V. Start Kit Product ID... On March 26, 2013 Covidien received a recall notice from one of their suppliers CareFusion. Care... Class III Covidien LLC
Apr 8, 2013 Medi-Trace Cadence Adult Radiotransparent Defibrillation Electrode Product I... Defibrillation Electrodes may arc/spark result in thermal damage to the leadwire, which could re... Class II Covidien LLC
Apr 8, 2013 Medi-Trace Cadence Pediatric Radiotransparent Defibrillation Electrode Produ... Defibrillation Electrodes may arc/spark result in thermal damage to the leadwire, which could re... Class II Covidien LLC
Aug 3, 2012 HALO Flex Energy Generators Manufactured by B¿RRX Medical (now Covidien) ... Potential failure of HALO Energy Generator to enter "stand by" mode when initially powered on; an... Class II Covidien LLC
Feb 9, 2012 Reusable, Self-Adhering TENS/NMES/FES electrodes Single Patient Use Only. ... Covidien is conducting a voluntary recall regarding specific lots of TENS electrodes because it w... Class II Covidien LLC dba Uni-Patch
Feb 9, 2012 Reusable, non-sterile, self-adhering electrodes for use with TENS/NMES, . Ma... Covidien is conducting a voluntary recall regarding specific lots of TENS electrodes because it w... Class II Covidien LLC dba Uni-Patch
Feb 9, 2012 Performa reusable and self-adhering TENS/NMES/FES stimulating electrodes, ... Covidien is conducting a voluntary recall regarding specific lots of TENS electrodes because it w... Class II Covidien LLC dba Uni-Patch
Feb 9, 2012 Empi STIMC RE Self Adhesive electrodes. For use on TENS, NMES, FES. a DJO b... Covidien is conducting a voluntary recall regarding specific lots of TENS electrodes because it w... Class II Covidien LLC dba Uni-Patch

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.