Zimmer Biomet recalls ceramic hip prosthesis heads with incompatible labeling for cobalt-chrome or stainless-steel stems. Affected units may not fit properly, risking improper joint function.
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.
Zimmer Biomet is recalling ceramic hip prosthesis heads that have labeling issues preventing proper compatibility with certain stems. This could lead to improper joint function if the prosthesis is used without correct matching.
The labeling does not clearly state which stems the ceramic head is compatible with. This could cause improper fitting with cobalt-chrome or stainless-steel stems, potentially leading to joint issues.
Patients who received this specific ceramic hip prosthesis head (model 802602202) during surgery are likely affected. Surgeons and patients using the prosthesis are at risk of improper joint function.
Check for the model number 802602202 on the ceramic hip prosthesis head. The product was sold with specific implant instructions (IFU) versions 87-6204-051-99 Rev D or earlier.
Look for the model number 802602202 on the ceramic hip prosthesis head.
The product labeling does not adequately provide compatibility information for use with cobalt-chrome or stainless-steel femoral stems.
Check the model number on the prosthesis head. If it matches 802602202, contact Zimmer Biomet for guidance.
The recall addresses potential improper fitting, but the official notice does not specify a risk of serious injury.
We’ve drafted a message you can send Zimmer to request your refund or repair — edit it as you like.
Subject: Recall Z-1645-2025 — Zimmer Zimmer Hello, I own a Zimmer that is covered by recall Z-1645-2025 from Zimmer. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
