Zimmer, Inc. recalls Zimmer Biomet Ceramic Head, 22.2 mm Diameter, Type 1, +3 Neck, Model Number 802802203; Prosthesis, Hip, Semi-Constraine…

Recall date

March 24, 2025

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-1649-2025

FDA classification

Class II

Brand / firm

Zimmer, Inc.

Sold / distributed

Worldwide distribution - US Nationwide and the countries of Panama, Hong Kong, China.

Why it was 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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Zimmer Biomet Ceramic Head, 22.2 mm Diameter, Type 1, +3 Neck, Model Number 802802203; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented or Non- Porous, Uncemented