FDA Medical devices recall ·
Zimmer Biomet Ceramic Head, 22.2 mm Diameter, Type 1, -3 Neck… recall
- Recall number
- Z-1647-2025
- Date
- (initiated March 24, 2025)
- Company / brand
- Zimmer, Inc.
1800 W Center St, Warsaw, IN, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 167 units
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Zimmer Biomet Ceramic Head, 22.2 mm Diameter, Type 1, -3 Neck, Model Number 802802201; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented or Non- Porous, Uncemented
Why was it 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.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
GTIN 00887868376344, All lots distributed with IFU 87-6204-051-99 Rev D or prior
Distribution
Worldwide distribution - US Nationwide and the countries of Panama, Hong Kong, China.
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-1647-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.