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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.

22,877medical device recall records
2,186FDA Class I records
8firms with 5+ records
Zimmer Biomet, Inc.736 records
Database records

Records — page 261

22,877 detailed records are currently available in this category.

Medical DeviceMay 22, 2024

HeartSine samaritan PAD recall — FDA Z-1820-2024

Automated external defibrillators have a manufacturing issue that could prevent the device from delivering instructional voice prompts to the user during use of the device. Visual…

Class IIFDA: OngoingHeartSine Technologies Ltd
Medical DeviceMay 22, 2024

TriMed recall — FDA Z-1792-2024

Nail system contains an out of specification driver-socket which could result in inability to pick up nails or apply sufficient torque.

Class IIFDA: OngoingTriMed 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.