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Browse Device Recalls

5 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 5 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 5 FDA device recalls.

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DateProductReasonClassFirm
Nov 16, 2015 Sodium Chloride Inhalation Solution, USP 7%, 60 x 4 mL Sterile Unit-Dose Vial... Lack of Assurance of Sterility: Internal dye ingress test failure to assure the integrity of the ... Class II Nephron Pharmaceuticals Corp.
Nov 16, 2015 Sodium Chloride Inhalation Solution, USP 3%, 60 x 4 mL Sterile Unit-Dose Vial... Lack of Assurance of Sterility: Internal dye ingress test failure to assure the integrity of the ... Class II Nephron Pharmaceuticals Corp.
Apr 30, 2013 AsthmaNefrin Starter Kit contains ten (10) AsthmaNefrin vials and one (1) EZ ... Possible dislodgement of the "Plate A", if this instance occurs, it presents a potential choking ... Class I Nephron Pharmaceuticals Corp.
Apr 30, 2013 EZ Breathe Atomizer Model # EZ-100. For the delivery of liquid medication... Possible dislodgement of the "Plate A", if this instance occurs, it presents a potential choking ... Class I Nephron Pharmaceuticals Corp.
Apr 30, 2013 EZ Breathe Medication Cup. For the delivery of liquid medications for resp... Possible dislodgement of the "Plate A", if this instance occurs, it presents a potential choking ... Class I Nephron Pharmaceuticals Corp.

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.