Zimmer Biomet recalls XP-CR Tibial Tray - Interlok 91mm (Item #195279) due to locking bar not fully engaging. This could lead to improper joint alignment during surgery. Affected units have specific lot numbers listed in the recall.
The locking bar not fully engaging
Zimmer Biomet is recalling XP-CR Tibial Tray - Interlok 91mm implants because the locking bar might not engage properly during surgery. This could cause improper joint alignment and potentially lead to complications for patients. The recall affects specific lot numbers of the product.
The locking bar not fully engaging could result in improper alignment of the knee joint during surgery. This might lead to complications such as instability or misalignment of the implant, which could require additional surgical corrections.
Orthopedic surgeons and medical facilities that use this specific implant during knee surgery are most at risk. Patients who have received this implant are not directly affected by the recall.
Check the product label for the item number 195279 and lot numbers listed: 262480, 960510, 274400, 274430, 336060, 336060R, 274390, 274410, 279280, 394540, 394590, 394570, 821400, 903420, 960530, 422490, 512590.
Look for the item number 195279 and the specific lot numbers listed in the recall.
No, this recall is for surgical implants used during procedures. Patients who have received the implant are not directly affected by this recall.
If you are a surgeon or medical facility using this product, check the product label for the item number and lot numbers listed in the recall. Contact Zimmer Biomet for further instructions.
Check the product label for the item number 195279 and the specific lot numbers listed: 262480, 960510, 274400, 274430, 336060, 336060R, 274390, 274410, 279280, 394540, 394590, 394570, 821400, 903420, 960530, 422490, 512590.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-2514-2019 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-2514-2019 from Zimmer Biomet. 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.
