Zimmer Biomet recalls ceramic hip prostheses with 22.2mm diameter heads that may not fit with certain stems, risking improper fit and injury. Affected units include specific model numbers and lots.
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 22.2 mm ceramic heads that may not be compatible with cobalt-chrome or stainless-steel femoral stems. This could lead to improper fit and potential injury during surgery or long-term use.
The ceramic heads may not fit properly with certain stem materials, leading to improper alignment or movement during use. This could cause pain, instability, or complications if the prosthesis is not correctly matched to the stem.
Patients who received the specific ceramic hip prosthesis model (22.2 mm diameter, Type 1, +0 neck, Model 802802202) from Zimmer Biomet are affected. Those with the prosthesis attached to cobalt-chrome or stainless-steel stems are at higher risk.
Check for the model number 802802202 on the ceramic head. The prosthesis was sold with specific IFU (instruction for use) versions 87-6204-051-99 Rev D or earlier. It was distributed with GTIN 00887868376351.
Verify the model number on the ceramic head is 802802202.
The product labeling does not adequately provide compatibility information for use with cobalt-chrome or stainless-steel femoral stems.
The recall does not specify a remedy, so contact Zimmer Biomet directly for guidance.
Yes, the affected model is 22.2 mm diameter, Type 1, +0 neck, Model Number 802802202.
We’ve drafted a message you can send Zimmer to request your refund or repair — edit it as you like.
Subject: Recall Z-1648-2025 — Zimmer Zimmer Hello, I own a Zimmer that is covered by recall Z-1648-2025 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.
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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.
