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Medical Device Recalls in the United States

Monitor U.S. medical device recall enforcement reports from the FDA. Review product descriptions, recall reasons, classifications, dates, recalling firms and distribution information where the FDA provides them.

21,924medical device recall records
2,160FDA Class I records
8firms with 5+ records
MEDLINE INDUSTRIES, LP…730 records
Database records

Records — page 106

21,924 detailed records are currently available in this category.

Medical DeviceOct 15, 2025

Inpeco S.A FlexLab (FLX) System recall — FDA Z-0106-2026

The FlexLab System Sample Integrity Module (SIM) includes function that determines the hemolysis, icterus, and lipemia (HIL) in blood samples. This function has not been evaluated for…

Class IIFDA: OngoingInpeco S.A.
Medical DeviceOct 15, 2025

NOXBOX recall — FDA Z-0029-2026

The unexpected internal fault / system diagnostic error to result when a rapid succession of button selections is made to the user interface without waiting for the device to respond to…

Class IFDA: OngoingNOXBOX LTD
Medical DeviceOct 8, 2025

Atlan A350 recall — FDA Z-2616-2025

The device either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.

Class IFDA: OngoingDraeger, Inc.

How to use this medical device recall index

Medical device recall records can change as the FDA receives additional information. Check the official record identifier and current FDA information before making health or product-use decisions.

Recall Lookup USA keeps the last complete source record available when an official data service is temporarily unavailable. When a source provides only a few fields, we show only those known facts rather than padding the page with generic text.

What the database can and cannot tell you

This database is designed for discovery and reference. It can help you locate a relevant recall record, identify the recalling firm or NHTSA campaign, compare dates and classifications, and follow the official source. It is not a substitute for a VIN-specific NHTSA check, a manufacturer notice, medical advice or instructions issued by the recalling company.