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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.

29,496medical device recall records
2,407FDA Class I records
8firms with 5+ records
Zimmer Biomet, Inc.784 records
Database records

Records — page 1115

29,496 detailed records are currently available in this category.

Medical DeviceFeb 17, 2016

Mizuho OSI Trios, Table Base recall — FDA Z-0792-2016

Table Bases may have been assembled incorrectly, missing a retaining ring from the head end assembly. Over time, the parts could go out of alignment, making clutch engagement or…

Class IIFDA: TerminatedMizuho OSI
Medical DeviceFeb 10, 2016

Philips Electronics INTEGRIS V3000 recall — FDA Z-0721-2016

The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ systems regarding live images and still images can lead to still images being interpreted as live Images.

Class IIFDA: TerminatedPhilips Electronics North America Corporation
Medical DeviceFeb 10, 2016

Philips Electronics Allura Xper FD10/10 recall — FDA Z-0703-2016

The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ systems regarding live images and still images can lead to still images being interpreted as live Images.

Class IIFDA: TerminatedPhilips Electronics North America Corporation
Medical DeviceFeb 10, 2016

Philips Electronics INTEGRIS CV recall — FDA Z-0729-2016

The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ systems regarding live images and still images can lead to still images being interpreted as live Images.

Class IIFDA: TerminatedPhilips Electronics North America Corporation
Medical DeviceFeb 10, 2016

Philips Electronics Allura Xper FD20/10 recall — FDA Z-0705-2016

The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ systems regarding live images and still images can lead to still images being interpreted as live Images.

Class IIFDA: TerminatedPhilips Electronics North America Corporation
Medical DeviceFeb 10, 2016

Philips Electronics INTEGRIS H5000 recall — FDA Z-0722-2016

The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ systems regarding live images and still images can lead to still images being interpreted as live Images.

Class IIFDA: TerminatedPhilips Electronics North America Corporation

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.