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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
Feb 27, 2019 MOOG Curlin Infusion Administration Set, REF 340-4130-V, Non-DEHP Tubing with... Administration sets leaked at the filter. Class II Zevex Incorporated (dba MOOG Medical Devices Gr...
Feb 27, 2019 MOOG Curlin Infusion Administration Set, REF 340-4130, Non-DEHP Tubing with N... Administration sets leaked at the filter. Class II Zevex Incorporated (dba MOOG Medical Devices Gr...
Dec 23, 2015 Moog Curlin Infusion, Ambulatory Infusion Pump The Curlin Ambulatory Infusi... Moog is recalling Curlin 4000, 6000, and PainSmart Infusion Pumps manufactured or serviced by MMD... Class II MOOG Medical Devices Group
Nov 20, 2015 Catalog No. INF0020-A  EnteraLite Infinity Enteral Pump Delivery Set with EN... Potential for leaking between the purple ENFit connector and the white transitional stepped conne... Class II MOOG Medical Devices Group
Nov 8, 2012 EnteraLite Infinity Enteral Feeding Pump identified with the following list n... MOOG Medical Devices Group is conducting a voluntary for a limited set of serial numbers of the E... Class II MOOG Medical Devices Group
Oct 12, 2012 Infinity Enteralite Ambulatory Feeding Pumps, List number: INFKIT2 - Addendum... The firm is adding an addendum to the operator's manual for Infinity Enteralite Ambulatory Feedin... Class II MOOG Medical Devices Group
Sep 26, 2012 ***This recall is being conducted due to an incomplete recall for RES 57829**... This recall is the same issue for the FDA processed recall initiated by Moog Medical Devices on 1... Class II MOOG Medical Devices Group

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.