Zimmer Biomet recalls Vanguard XP Tibial Tray 73mm (Item #195250) due to locking bar not fully engaging, which could lead to improper fixation during surgery. Affected items have specific lot numbers.
The locking bar not fully engaging
Zimmer Biomet is recalling Vanguard XP Tibial Tray 73mm (Item #195:250) because the locking bar may not fully engage, potentially causing improper fixation during surgery. This recall affects specific lot numbers of the product.
The locking bar not fully engaging could result in the implant not staying securely in place during surgery. This might cause improper fixation of the knee joint, leading to potential complications after the procedure.
Orthopedic surgeons and medical facilities that use this specific implant during knee replacement surgery. Patients who have received this implant are not directly affected by the recall.
Check for the product name 'Vanguard XP Tibial Tray 73mm' with item number 195250. Affected items have specific lot numbers listed in the recall notice.
Verify the item number and lot numbers listed in the recall notice to confirm if your product is affected.
The recall indicates a potential issue with the locking bar not fully engaging, so it is not recommended for use until the recall is addressed.
Check the item number and lot numbers provided in the recall notice to determine if your product is affected. If affected, contact Zimmer Biomet for further instructions.
Look for the product name 'Vanguard XP Tibial Tray 73mm' with item number 195250 and specific lot numbers listed in the recall 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-2533-2019 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-2533-2019 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.
