Zimmer Biomet recalls XP-XP Tibial Tray - Interlok 65mm (Item #195752) due to locking bar not fully engaging, which could lead to improper fixation during surgery. Affected items have specific lot numbers.
The locking bar not fully engaging
Zimmer Biomet is recalling XP-XP Tibial Tray - Interlok 65mm implants (Item #195752) because the locking bar might not engage properly during surgery. This could cause improper fixation of the implant, potentially leading to complications for patients.
The locking bar may not fully engage during surgery, which could result in the implant not staying securely in place. This might cause improper fixation and potential complications for the patient.
Orthopedic surgeons and patients who have received the XP-XP Tibial Tray - Interlok 65mm implant (Item #195752) with specific lot numbers. Patients are at risk if the implant does not fix properly during surgery.
Check the product label for the model 'XP-XP Tibial Tray - Interlok 65mm' and item number 195752. Affected items have specific lot numbers listed in the recall notice.
Look for the model 'XP-XP Tibial Tray - Interlok 65mm' and item number 195752 on the product label.
The locking bar may not fully engage during surgery, which could result in improper fixation of the implant.
Check the product label for the model 'XP-XP Tibial Tray - Interlok 65mm' and item number 195752. Affected items have specific lot numbers listed in the recall notice.
The recall does not specify a remedy, so contact Zimmer Biomet directly for further instructions.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-2525-2019 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-2525-2019 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.
