Zimmer Biomet recalls Vanguard XP Tibial Tray 87mm (Item #195254) due to potential locking bar failure. No units distributed.
The locking bar not fully engaging
Zimmer Biomet is recalling a specific orthopedic implant model because its locking mechanism may not engage properly. This could lead to improper fixation during surgery, but no units have been distributed.
The locking bar not fully engaging could cause the implant to become loose during surgery. This might lead to improper fixation of the bone, potentially requiring additional surgery or causing complications.
Orthopedic surgeons and hospitals that might use this implant are affected. Patients receiving this specific implant during surgery are at risk.
Check for the Vanguard XP Tibial Tray 87mm with item number 195254. No units have been distributed, so this recall does not affect any current users.
Verify if your implant matches the Vanguard XP Tibial Tray 87mm with item number 195254.
No units have been distributed, so this recall does not affect any current users.
Since no units have been distributed, there is no action required for this recall.
The recall states the locking bar may not engage properly, but no units have been distributed, so the risk is currently unknown.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-2537-2019 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-2537-2019 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.
