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Browse Device Recalls

7 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 7 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 7 FDA device recalls.

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DateProductReasonClassFirm
Aug 15, 2019 Grab n Go Opti series VIPR system Model # PRX-9615 - Product Usage: The Gra... Limited access to flow settings as a result of the control knob having been rotated beyond its f... Class II Western / Scott Fetzer Company
Aug 15, 2019 Grab n Go Opti series VIPR system Model # PRX-9627 - Product Usage: The Gra... Limited access to flow settings as a result of the control knob having been rotated beyond its f... Class II Western / Scott Fetzer Company
Aug 15, 2019 Grab n Go Opti series VIPR system Model # PRX-9632 - Product Usage: The Gra... Limited access to flow settings as a result of the control knob having been rotated beyond its f... Class II Western / Scott Fetzer Company
Aug 15, 2019 Grab n Go Opti series VIPR system Model # PRX-9653 - Product Usage: The Gra... Limited access to flow settings as a result of the control knob having been rotated beyond its f... Class II Western / Scott Fetzer Company
Aug 15, 2019 Grab n Go Opti series VIPR system Model # PRX-9646 - Product Usage: The Gra... Limited access to flow settings as a result of the control knob having been rotated beyond its f... Class II Western / Scott Fetzer Company
Jan 31, 2015 Various OxyTOTE Portable Oxygen System regulators, Valve Integrated Pressure ... The firm has become aware of the possibility of ignition and rupture (explosion) of a compressed ... Class I Western / Scott Fetzer Company
Apr 7, 2014 Model RG3000 and RG4000 Series Valve Integrated Pressure Regulator (VIPR) Separation events have occurred, including the VIPR separating from the Aluminum cylinder. Class II Western / Scott Fetzer Company

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.