Zimmer Biomet recalls XP-CR Tibial Tray - Interlok 73mm Item # 195274 due to locking bar not fully engaging, which may cause improper fit during surgery.
The locking bar not fully engaging
Zimmer Biomet is recalling XP-CR Tibial Tray - Interlok 73mm implants because the locking bar might not engage properly during surgery. This could lead to improper implant positioning and potential complications for patients.
The locking bar may not fully engage, which can cause the implant to become improperly positioned during surgery. This could lead to complications such as improper bone alignment or the need for additional surgical corrections.
Orthopedic surgeons and their patients who have received the specific XP-CR Tibial Tray - Interlok 73mm implant (Item # 195274) from the listed lot numbers. Patients using this implant during surgery are at risk.
Check if your implant has the model name 'XP-CR Tibial Tray - Interlok 73mm' and the specific item number 195274. Lot numbers listed in the recall include 553880, 590760, and other numbers provided in the recall notice.
Identify if your implant matches the model name 'XP-CR Tibial Tray - Interlok 73mm' and item number 195274.
The recall states the locking bar may not fully engage, which could lead to improper implant positioning during surgery. However, the specific risk level is not clearly described in the notice.
The recall does not specify a remedy, so you should contact Zimmer Biomet directly for further instructions.
Check the model name 'XP-CR Tibial Tray - Interlok 73mm' and item number 195274. Lot numbers listed in the recall include several specific numbers like 553880 and 590760.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-2509-2019 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-2509-2019 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.
