Zimmer Biomet Vanguard XP Tibial Tray 63mm Recall: Locking Bar Not Fully Engaging

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Recalling firmZimmer Biomet, Inc.56 E Bell Dr · Warsaw, IN 46582-6989

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Zimmer Biomet is recalling Vanguard XP Tibial Tray 63mm implants (Item #19524: 195245) because the locking bar may not engage properly. This could cause improper fixation during surgery, potentially leading to complications for patients.

Why it’s dangerous

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, potentially leading to surgical complications.

Who’s affected

Orthopedic surgeons and their patients who have received the recalled Vanguard XP Tibial Tray 63mm implants. Patients undergoing knee replacement surgery are most at risk.

How to tell if you have this one

Check for the product name 'Vanguard XP Tibial Tray 63mm' and item number 195245. The recall includes specific lot numbers: 833140, 332580, 514890, 764300, 754440, 837720, 999580, 999590, 999570, 764290, 999610, 090060, 090020.

Brand
Zimmer Biomet
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Verify the product name and item number on the implant packaging or documentation.

✎ GovInfoNow

Questions people ask

Is this recall affecting my surgery?

This recall applies to specific implants used in knee replacement surgery. If you have the recalled Vanguard XP Tibial Tray 63mm, contact your surgeon for guidance.

How can I tell if my implant is recalled?

Check for the product name 'Vanguard XP Tibial Tray 63mm' and item number 195245. The recall includes specific lot numbers listed in the notice.

What should I do if I have the recalled implant?

The recall does not specify a remedy, so contact your surgeon to discuss next steps for the implant.

Take action

Contact Zimmer Biomet

We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-2528-2019 — Zimmer Biomet Zimmer Biomet

Hello,

I own a Zimmer Biomet that is covered by recall Z-2528-2019 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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Where this comes from

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.

Official source: FDA Recall #Z-2528-2019 (August 15, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2528-2019 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Zimmer Biomet, Inc. recalls Vanguard XP Tibial Tray 63 mm Item # 195245

Recall notice