PlainRecalls
FDA Devices Moderate Class II Ongoing

Zimmer Biomet Ceramic Head, 22.2 mm Diameter, Type 1, +0 Neck, Model Number 802802202; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented or Non- Porous, Uncemented

Reported: April 30, 2025 Initiated: March 24, 2025 #Z-1648-2025

Product Description

Zimmer Biomet Ceramic Head, 22.2 mm Diameter, Type 1, +0 Neck, Model Number 802802202; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented or Non- Porous, Uncemented

Reason for Recall

The associated product labeling does not adequately provide compatibility information for use of the 22.2 mm Diameter Ceramic Femoral Heads with cobalt-chrome femoral stems or stainless-steel femoral stems.

Details

Recalling Firm
Zimmer, Inc.
Units Affected
158 units
Distribution
Worldwide distribution - US Nationwide and the countries of Panama, Hong Kong, China.
Location
Warsaw, IN

Frequently Asked Questions

What product was recalled?
Zimmer Biomet Ceramic Head, 22.2 mm Diameter, Type 1, +0 Neck, Model Number 802802202; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented or Non- Porous, Uncemented. Recalled by Zimmer, Inc.. Units affected: 158 units.
Why was this product recalled?
The associated product labeling does not adequately provide compatibility information for use of the 22.2 mm Diameter Ceramic Femoral Heads with cobalt-chrome femoral stems or stainless-steel femoral stems.
Which agency issued this recall?
This recall was issued by the FDA Devices on April 30, 2025. Severity: Moderate. Recall number: Z-1648-2025.