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Browse Device Recalls

3 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 3 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 3 FDA device recalls.

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DateProductReasonClassFirm
Jul 10, 2017 Purely Yours Breast Pump. Model 17070PMW and Model 17070ACA. Intended to ... Two specific lots was incorrectly manufactured containing a UK power adapter. Class III AMEDA, INC.
Feb 12, 2015 Ameda One-Hand Manual Breast Pump (SKU 17161) - Primary packaging is 6 pouche... Devices were not sterilized Class II Ameda, Inc.
Feb 12, 2015 Ameda Dual Short Term HygieniKit Milk Collections System (SKU 17115) - Primar... Devices were not sterilized Class II Ameda, Inc.

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.