Zimmer Biomet recalls XP-CR Tibial Tray - Interlok 65mm (Item #195270) due to locking bar not fully engaging, which could lead to improper fixation during surgery. Affected units include specific lot numbers listed in the recall notice.
The locking bar not fully engaging
Zimmer Biomet is recalling XP-CR Tibial Tray - Interlok 65mm (Item #195270) because the locking bar may not fully engage, potentially causing improper fixation during surgery. This could lead to complications for patients undergoing orthopedic procedures.
The locking bar not fully engaging could result in the implant not staying securely in place during surgery. This might cause improper fixation of the bone, leading to potential complications like displacement or failure of the implant after surgery.
Orthopedic surgeons and surgical teams using the XP-CR Tibial Tray - Interlok 65mm implant during procedures. Patients who have received this implant are at risk if the locking bar fails to engage properly.
Check for the product name 'XP-CR Tibial Tray - Interlok 65mm' and item number 195270. Affected units include specific lot numbers listed in the recall notice, such as 666880, 660440, and others.
Reach out to Zimmer Biomet directly to confirm if your specific lot number is affected and to get instructions for next steps.
The recall indicates a potential hazard, so affected units should not be used until further instructions are received from Zimmer Biomet.
Contact Zimmer Biomet to determine if your specific lot number is affected and follow their instructions.
Check the lot numbers listed in the recall notice (e.g., 666880, 660440) to see if your product matches the affected units.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-2505-2019 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-2505-2019 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.
