Medical Device Recalls

This is our largest category by volume. The FDA tracks recalls for an enormous range of medical devices: implants, pacemakers, insulin pumps, surgical tools, blood glucose monitors, X-ray machines, prosthetics, contact lenses, and home health equipment, among many others. We have records dating back to 2005 and add new ones as the FDA publishes them.

Device recalls can happen because of software bugs, manufacturing defects, bacterial contamination, incorrect labeling, or design flaws that lead to inaccurate results or equipment failure. Class I recalls are the most serious and mean the device could cause injury or death.

38,428 total recalls
0 this month

Showing 20401–20420 of 38,428 recalls

July 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Left 125¿ 9 mm x 320 mm

The Issue: The set screw is not able to advance

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
July 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Left 125¿ 11 mm x 400 mm

The Issue: The set screw is not able to advance

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
July 16, 2018· Valeris Medical, LLC

Recalled Item: Valeris Medical Apollo Medial Suture Anchor

The Issue: Mislabeling

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
July 16, 2018· Philips Electronics North America Corporation

Recalled Item: AIIuraXperFDlO/10

The Issue: There is a potential for the Monitor Ceiling

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
July 16, 2018· Philips Electronics North America Corporation

Recalled Item: INTEGRIS CV

The Issue: There is a potential for the Monitor Ceiling

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
July 16, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD1O C

The Issue: There is a potential for the Monitor Ceiling

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
July 16, 2018· Philips Electronics North America Corporation

Recalled Item: Poly C- DMCP-Visub(H3000)

The Issue: There is a potential for the Monitor Ceiling

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
July 16, 2018· Philips Electronics North America Corporation

Recalled Item: INTEGRIS SUITE

The Issue: There is a potential for the Monitor Ceiling

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
July 16, 2018· Philips Electronics North America Corporation

Recalled Item: AIIura Xper F010 DR Table

The Issue: There is a potential for the Monitor Ceiling

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
July 16, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD2O

The Issue: There is a potential for the Monitor Ceiling

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
July 16, 2018· Philips Electronics North America Corporation

Recalled Item: INTEGRIS Allura 9 (biplane)

The Issue: There is a potential for the Monitor Ceiling

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
July 16, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD2O

The Issue: There is a potential for the Monitor Ceiling

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
July 16, 2018· Philips Electronics North America Corporation

Recalled Item: INTEGRIS Allura 15-12 (mono)

The Issue: There is a potential for the Monitor Ceiling

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
July 16, 2018· Philips Electronics North America Corporation

Recalled Item: NTEGRIS Allura 9 0 FDXD

The Issue: There is a potential for the Monitor Ceiling

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
July 16, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper F010/10 DRTable

The Issue: There is a potential for the Monitor Ceiling

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
July 16, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD2O Biplane

The Issue: There is a potential for the Monitor Ceiling

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
July 16, 2018· Philips Electronics North America Corporation

Recalled Item: AlIura Xper F010 F

The Issue: There is a potential for the Monitor Ceiling

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
July 16, 2018· Philips Electronics North America Corporation

Recalled Item: INTEGRIS Allura 9

The Issue: There is a potential for the Monitor Ceiling

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
July 16, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper F020 DR Table

The Issue: There is a potential for the Monitor Ceiling

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
July 16, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper F010 DR Table

The Issue: There is a potential for the Monitor Ceiling

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated