Zimmer Biomet recalls Vanguard XP Tibial Tray 71 mm (Item #195249) 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 Vanguard XP Tibial Tray 71 mm (Item #195:249) because the locking bar might not engage properly. This could lead to improper fixation during surgery, potentially causing complications for patients.
The locking bar not fully engaging could cause the tibial tray to become loose during surgery. This might lead to improper fixation of the implant, potentially causing complications like instability or displacement.
Orthopedic surgeons and their patients who used the recalled Vanguard XP Tibial Tray 71 mm during surgery. Patients are at risk if the implant doesn't stay securely in place.
Check for the product name 'Vanguard XP Tibial Tray 71 mm' and item number 195249. Affected units have specific lot numbers listed in the recall notice.
Reach out to Zimmer Biomet for specific instructions on how to handle the recalled item.
The recall indicates a potential issue with the locking bar, so it is not recommended for use until the manufacturer provides instructions.
Contact Zimmer Biomet directly for details on the recall and next steps.
Yes, the recall includes specific lot numbers such as 584220, 590500, and others listed in the notice.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-2532-2019 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-2532-2019 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
