Zimmer Biomet recalls XP-XP Tibial Tray - Interlok 71 mm (Item #195755) due to locking bar not fully engaging. Affected units have specific lot numbers. Consumers should contact Zimmer Biomet for details.
The locking bar not fully engaging
Zimmer Biomet is recalling XP-XP Tibial Tray - Interlok 71 mm (Item #195755) because the locking bar may not fully engage, potentially causing instability during surgery. This could lead to complications if the implant shifts during use.
The locking bar not fully engaging could cause the implant to shift or become unstable during surgery. This instability might lead to complications such as improper alignment or the need for additional surgical corrections.
Orthopedic surgeons and medical professionals who use this specific implant during knee replacement surgeries are most at risk. Patients who have received this implant are not directly affected by the recall.
Check for the product name 'XP-XP Tibial Tray - Interlok 71 mm' with Item #195755. Affected units have specific lot numbers listed in the recall notice.
Reach out to Zimmer Biomet directly for specific instructions on how to verify your product and get further assistance.
No, this recall is for medical professionals using the implant during surgery. Patients who have received this implant are not affected by the recall.
Check for the product name 'XP-XP Tibial Tray - Interlok 71 mm' with Item #195755. Affected units have specific lot numbers listed in the recall notice.
Contact Zimmer Biomet directly for specific instructions on how to verify your product and get further assistance.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-2522-2019 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-2522-2019 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.
