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Zimmer Biomet, Inc.

Zimmer Biomet, Inc. Recalls

All product recalls associated with Zimmer Biomet, Inc..

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Recall Summary

Total Recalls

111

Past Year

Class I (Serious)

Most Recent

Oct 2023

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 101–111 of 111 recalls

Zimmer Biomet, Inc.: XP-CR Tibial Tray - Interlok 83 mm Item # 195277

The locking bar not fully engaging

FDAAug 15, 2019AL, AZ, AR +41 more• Zimmer Biomet, Inc.

Zimmer Biomet, Inc.: ASI 2.0 Calcar Trimmer Shaft for Use with Biomet Rasp, Mo...

The potential that the end of the shaft could fail to effectively mate with the broach with the Calcar Planar Shaft instrument, part number 110032331.

FDAAug 6, 2019AR, CA, CO +8 more• Zimmer Biomet, Inc.

Zimmer Biomet, Inc.: Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item #...

Cleaning processes potentially being ineffective

FDAJul 2, 2019AZ, CA, GA +16 more• Zimmer Biomet, Inc.

1...4 56

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Zimmer Biomet, Inc.: Comprehensive Reverse Shoulder Instrument Case Outer (Ou...

Lack of an adequate sterilization validation.

FDAJun 10, 2019Nationwide• Zimmer Biomet, Inc.

Zimmer Biomet, Inc.: Ultra-Drive Irrigation Tubing Assembly, Reference Number ...

The products do not have sufficient data to support the labeled shelf life of 10 years.

FDAJun 4, 2019Nationwide• Zimmer Biomet, Inc.

Zimmer Biomet, Inc.: Ultra-Drive Hose/Drape Assembly, Reference Number 423833 ...

The products do not have sufficient data to support the labeled shelf life of 10 years.

FDAJun 4, 2019Nationwide• Zimmer Biomet, Inc.

Zimmer Biomet, Inc.: K-Wire Trochar Tip, Model Number 212000008 Product Usa...

There is a potential for weak seals of the sterile packaging.

FDAMay 28, 2019Nationwide• Zimmer Biomet, Inc.

Zimmer Biomet, Inc.: DVR Crosslock ePAK Screw Driver, Model Number 212000002 ...

There is a potential for weak seals of the sterile packaging.

FDAMay 28, 2019Nationwide• Zimmer Biomet, Inc.

Zimmer Biomet, Inc.: DVR Crosslock ePAK Depth Gauge, Model Number 212000003 ...

There is a potential for weak seals of the sterile packaging.

FDAMay 28, 2019Nationwide• Zimmer Biomet, Inc.

Zimmer Biomet, Inc.: ROSA Surgical Device 2.5.8, a computer-controlled electro...

Potential failure of a force feedback sensor that may result in continued movement of an operating arm (rather than an immediate stop as intended).

Class IIModerate

FDANov 6, 2014AR, GA, IN +3 more• Zimmer Biomet, Inc.

Zimmer Biomet, Inc.: ROSA Surgical Device 2.5.8 ROSA Surgical Device is a com...

The software issue described was corrected in the modification to the MXTTOUT controller parameter settings.

Class IIModerate

FDASep 5, 2014Nationwide• Zimmer Biomet, Inc.