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Browse Device Recalls

63 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 63 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 63 FDA device recalls.

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DateProductReasonClassFirm
Apr 27, 2017 AirLife Resuscitation, Pediatric, with mask, 40inch oxygen reservoir tubing, ... The mask component on various lots of the resuscitation devices have been identified as having th... Class I Vyaire Medical
Apr 27, 2017 AirLife Resuscitation, Infant, with mask, oxygen reservoir bag, pressure-reli... The mask component on various lots of the resuscitation devices have been identified as having th... Class I Vyaire Medical
Apr 27, 2017 AirLife Resuscitation, Adult, with mask, oxygen reservoir bag, CO2 detector, ... The mask component on various lots of the resuscitation devices have been identified as having th... Class I Vyaire Medical
Apr 27, 2017 AirLife Resuscitation, Pediatric, with mask, 40inch oxygen reservoir tubing, ... The mask component on various lots of the resuscitation devices have been identified as having th... Class I Vyaire Medical
Apr 27, 2017 AirLife Resuscitation, Adult, with mask, 28inch large bore tubing, pressure-r... The mask component on various lots of the resuscitation devices have been identified as having th... Class I Vyaire Medical
Apr 27, 2017 AirLife Resuscitation, Infant, with mask, 40inch oxygen reservoir tubing, pre... The mask component on various lots of the resuscitation devices have been identified as having th... Class I Vyaire Medical
Apr 27, 2017 AirLife Resuscitation, Adult, with mask, oxygen reservoir bag, manometer P... The mask component on various lots of the resuscitation devices have been identified as having th... Class I Vyaire Medical
Apr 27, 2017 AirLife Resuscitation, Adult, with mask, oxygen reservoir bag, CO2 detector, ... The mask component on various lots of the resuscitation devices have been identified as having th... Class I Vyaire Medical
Apr 27, 2017 AirLife Resuscitation, Infant, with mask, 40inch oxygen reservoir tubing, pre... The mask component on various lots of the resuscitation devices have been identified as having th... Class I Vyaire Medical
Nov 29, 2014 Adult Air-Life single-limb circuit (Model AH202) with AirLife Humidification ... Manufacturing error in humidification chamber may cause an overfill/overflow condition of the cha... Class I Vyaire Medical
Nov 29, 2014 Infant AirLife Dual-,limb, dual-heat, high-flow circuit (Model AH265) with Ai... Manufacturing error in humidification chamber may cause an overfill/overflow condition of the cha... Class I Vyaire Medical
Nov 29, 2014 Infant AirLife single-limb, continuous-flow circuit (Model AH132) containing ... Manufacturing error in humidification chamber may cause an overfill/overflow condition of the cha... Class I Vyaire Medical
Nov 29, 2014 Adult AirLife dual-limb, dual-heat circuit (Model AH280) with AirLife Humidif... Manufacturing error in humidification chamber may cause an overfill/overflow condition of the cha... Class I Vyaire Medical

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.