Zimmer Biomet recalls XP-CR Tibial Tray - Interlok 67mm (Item #195271) due to locking bar not fully engaging, which could lead to improper fixation during surgery.
The locking bar not fully engaging
Zimmer Biomet is recalling XP-CR Tibial Tray - Interlok 67mm implants because the locking bar may not engage properly, potentially causing improper fixation during surgery. This recall affects surgeons and medical facilities using these specific implants.
The locking bar may not fully engage during surgical implantation, which could lead to improper fixation of the implant in the bone. This might cause the implant to shift or become unstable during healing, potentially affecting surgical outcomes.
Surgeons and medical facilities that use the recalled XP-CR Tibial Tray - Interlok 67mm implants are most at risk. The recall applies to specific lot numbers produced between 2000 and 2023.
Check the product label for the model 'XP-CR Tibial Tray - Interlok 67mm' and item number 195271. The recall includes specific lot numbers listed in the record, which were produced between 2000 and 2023.
Look for the model 'XP-CR Tibial Tray - Interlok 67mm' and item number 195271 on the product.
The recall is for a potential issue with the locking bar not fully engaging, which could lead to improper fixation during surgery. However, the hazard is considered low risk as it does not cause immediate injury in normal use.
Check the product label for the model and item number. If it matches the recalled items, contact Zimmer Biomet for further instructions.
The recalled product has the model 'XP-CR Tibial Tray - Interlok 67mm' and item number 195271. Check the lot numbers listed in the recall record.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-2506-2019 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-2506-2019 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.
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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.
