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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 61–80 of 111 recalls

Zimmer Biomet, Inc.: HA Pins (DFS HA Cort Screw), Hoffman/Colles Pins (Colles ...

Elevated levels of bacterial endotoxin and residual debris remain on the devices due to cleaning issue.

FDAAug 21, 2019Nationwide• Zimmer Biomet, Inc.

Zimmer Biomet, Inc.: HENNESSY LEFT CONST GLENOID HA, Item No. PM555360 UDI (0...

Elevated levels of bacterial endotoxin and residual debris remain on the devices due to cleaning issue.

FDAAug 21, 2019Nationwide• Zimmer Biomet, Inc.

Zimmer Biomet, Inc.: Compress, Mini Compress; Item Nos. 178350 178351 178352...

Elevated levels of bacterial endotoxin and residual debris remain on the devices due to cleaning issue.

FDAAug 21, 2019Nationwide

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• Zimmer Biomet, Inc.

Zimmer Biomet, Inc.: Various Hip systems, Item Nos. 104207 104212 104215 11...

Elevated levels of bacterial endotoxin and residual debris remain on the devices due to cleaning issue.

FDAAug 21, 2019Nationwide• Zimmer Biomet, Inc.

Zimmer Biomet, Inc.: Comprehensive RS Cleat CAP, Item No. 110300

Elevated levels of bacterial endotoxin and residual debris remain on the devices due to cleaning issue.

FDAAug 21, 2019Nationwide• Zimmer Biomet, Inc.

Zimmer Biomet, Inc.: Copeland HA Resurfacing Head, MB/HA EAS Head; Item Nos. 1...

Elevated levels of bacterial endotoxin and residual debris remain on the devices due to cleaning issue.

FDAAug 21, 2019Nationwide• Zimmer Biomet, Inc.