Zimmer Biomet recalls XP-CR Tibial Tray - Interlok 79mm (Item #195276) due to locking bar not fully engaging. This could lead to improper implant fixation. Affected units include specific lot numbers.
The locking bar not fully engaging
Zimmer Biomet is recalling XP-CR Tibial Tray - Interlok 7:99mm models with item number 195276 because the locking bar may not fully engage. This could cause improper implant fixation and potential complications during surgery.
The locking bar not fully engaging could lead to improper fixation of the implant in the bone. This might cause the implant to shift during surgery or after the procedure, potentially requiring additional corrective steps.
Orthopedic surgeons and medical professionals who use these implants during knee replacement surgeries. Patients receiving these implants are not directly affected by the recall.
Check for the product name 'XP-CR Tibial Tray - Interlok 79 mm' and item number 195276. Affected units have specific lot numbers listed in the recall notice.
Verify the item number and lot numbers listed in the recall notice to confirm if your implant is affected.
No, this recall is for surgical implants used during procedures. Patients who have already received the implant are not affected by this recall.
Check the item number and lot numbers listed in the recall notice to confirm if your implant is affected. If it is, contact Zimmer Biomet for further instructions.
Look for the product name 'XP-CR Tibial Tray - Interlok 79 mm' and item number 195276 on the implant. Check the lot numbers listed in the recall notice to confirm if it is affected.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-2511-2019 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-2511-2019 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.
