Zimmer Biomet recalls ceramic hip prostheses with model 802802201 due to unclear labeling on compatibility with metal and stainless steel stems. Affected users should contact Zimmer for guidance.
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 hip prostheses with model number 802802201 because the product labels don't clearly state which stems they're compatible with. This could lead to improper use if the prosthesis is paired with the wrong stem type.
The product labels don't provide enough information about which types of stems (cobalt-chrome or stainless-steel) the ceramic head is compatible with. This could lead to improper fitting if the prosthesis is used with an incompatible stem.
People who own or use Zimmer Biomet hip prostheses with model number 802802201 are affected. Those with metal or stainless-steel stems may be at higher risk if the prosthesis isn't compatible.
Check for the model number 802802201 on the hip prosthesis. The product was sold with specific instructions (IFU) versions 87-6204-051-99 Rev D or earlier.
Look for the model number 802802201 on the hip prosthesis to confirm if it's affected.
The recall is for labeling issues, not a direct safety hazard. The product may not fit properly with certain stems, but this is not an immediate risk.
Check for the model number 802802201 on the prosthesis. The product was sold with instructions (IFU) versions 87-6204-051-99 Rev D or earlier.
Contact Zimmer Biomet directly for guidance on compatibility with your stem type.
We’ve drafted a message you can send Zimmer to request your refund or repair — edit it as you like.
Subject: Recall Z-1647-2025 — Zimmer Zimmer Hello, I own a Zimmer that is covered by recall Z-1647-2025 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.
