Zimmer Biomet recalls XP-CR Tibial Tray - Interlok 71mm (Item #195273) due to locking bar not fully engaging, which could lead to improper joint stability during surgery.
The locking bar not fully engaging
Zimmer Biomet is recalling XP-CR Tibial Tray - Interlok 71mm implants because the locking bar might not engage properly. This could cause improper joint stability during surgery, potentially leading to complications for patients.
The locking bar not fully engaging could result in the implant not staying securely in place during surgery. This might cause improper joint alignment, leading to potential complications such as instability or misalignment of the knee joint.
Orthopedic surgeons and patients who have received the specific XP-CR Tibial Tray - Interlok 71mm implant (Item #195273) are affected. Patients who have undergone knee surgery with this implant are most at risk.
Check if your implant has the model name 'XP-CR Tibial Tray - Interlok 71mm' and the specific item number 195273. The recall includes implants with various lot numbers listed in the record.
Reach out to Zimmer Biomet directly to confirm if your implant is affected and get instructions for next steps.
This recall specifically affects XP-CR Tibial Tray - Interlok 71mm implants with item number 195273. If you have this specific implant, contact Zimmer Biomet to confirm.
Contact Zimmer Biomet directly to determine if your implant is affected and follow their instructions for next steps.
Check the product name and item number on your implant. The recall includes XP-CR Tibial Tray - Interlok 71mm with item number 195273 and specific lot numbers listed in the 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-2508-2019 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-2508-2019 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.
