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 17041–17060 of 38,428 recalls

August 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-CR Tibial Tray - Interlok 83 mm Item # 195277

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardTerminated
August 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-XP Tibial Tray - Interlok 67 mm Item # 195753

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardTerminated
August 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-XP Tibial Tray - Interlok 69 mm Item # 195754

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardTerminated
August 15, 2019· Zimmer Biomet, Inc.

Recalled Item: Vanguard XP Tibial Tray 65 mm Item # 195246

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardTerminated
August 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-CR Tibial Tray - Interlok 63mm Item # 195269

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardTerminated
August 15, 2019· Zimmer Biomet, Inc.

Recalled Item: Vanguard XP Tibial Tray 69 mm Item # 195248

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardTerminated
August 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-XP Tibial Tray - Interlok 75 mm Item # 195757

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardTerminated
August 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-CR Tibial Tray - Interlok 71mm Item # 195273

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardTerminated
August 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-CR Tibial Tray - Interlok 65mm Item # 195270

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardTerminated
August 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-CR Tibial Tray - Interlok 73mm Item # 195274

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardTerminated
August 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-CR Tibial Tray - Interlok 79 mm Item # 195276

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardTerminated
August 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-XP Tibial Tray - Interlok 63 mm Item # 195751

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardTerminated
August 15, 2019· Zimmer Biomet, Inc.

Recalled Item: Vanguard XP Tibial Tray 71 mm Item # 195249

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardTerminated
August 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-XP Tibial Tray - Interlok 71 mm Item # 195755

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardTerminated
August 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP- CR Tibial Tray- Interlok 59mm Item # 195268

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardTerminated
August 15, 2019· Zimmer Biomet, Inc.

Recalled Item: Vanguard XP Tibial Tray 87 mm Item # 195254

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardTerminated
August 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-XP Tibial Tray - Interlok 87 mm Item # 195760

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardTerminated
August 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-CR Tibial Tray - Interlok 67mm Item # 195271

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardTerminated
August 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-CR Tibial Tray - Interlok 69mm Item # 195272

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardTerminated
August 15, 2019· Zimmer Biomet, Inc.

Recalled Item: Vanguard XP Tibial Tray 83 mm Item # 195253

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardTerminated