Zimmer Biomet recalls Vanguard XP Tibial Tray 67mm (Item #195247) due to locking bar not fully engaging. Affected items 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 67mm (Item #195:247) because the locking bar may not fully engage. This could lead to improper fixation during surgery, potentially causing complications for patients.
The locking bar may not fully engage, which could cause the implant to become loose during surgery. This might lead to improper fixation of the bone, potentially causing complications like pain or the need for additional surgery.
Orthopedic surgeons and their patients who used the recalled Vanguard XP Tibial Tray 67mm during surgery. Patients are at risk if the implant does not stay securely in place during the procedure.
Check for the product name 'Vanguard XP Tibial Tray 67mm' with Item #195247. Affected items have specific lot numbers: 332640, 372960, 514940, and other numbers listed in the recall notice.
Reach out to Zimmer Biomet directly for specific instructions on how to handle the recalled item.
The recall indicates a potential issue with the locking bar not fully engaging, so it is not recommended for use until the manufacturer provides instructions.
Check for the product name 'Vanguard XP Tibial Tray 67mm' with Item #195247 and specific lot numbers listed in the recall notice.
Contact Zimmer Biomet directly for specific instructions on how to handle the recalled item.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-2530-2019 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-2530-2019 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.
