Zimmer Biomet Vanguard XP Tibial Tray 83mm 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 83mm (Item #195:253) because the locking bar may not engage fully. This could lead to improper fixation during surgery, potentially causing complications for patients.

Why it’s dangerous

The locking bar not fully engaging could result in the tibial tray not staying securely in place during surgery. This might cause the implant to shift, leading to potential complications for the patient.

Who’s affected

Orthopedic surgeons and their patients who have received the recalled Vanguard XP Tibial Tray 83mm (Item #195253) during surgery. Patients using the implant are at risk of improper fixation.

How to tell if you have this one

Check for the product name 'Vanguard XP Tibial Tray 83mm' and item number 195253. Affected items have specific lot numbers: 332760, 752520, 515140, 754520, 063070, 072460, 072440, 072510, 663350, 663360, 833240, 919270, 764460, 846570, 764450, 837820, 861240, 915690, 915700.

Brand
Zimmer Biomet
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Contact Manufacturer
Reach out to Zimmer Biomet directly for specific instructions on handling the recalled item.

✎ GovInfoNow

Questions people ask

Is this product safe to use?

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.

What should I do if I have this product?

Contact Zimmer Biomet for details on the recall and next steps.

How can I check if my product is affected?

Check for the product name 'Vanguard XP Tibial Tray 83mm' and item number 195253 with the listed lot numbers.

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-2536-2019 — Zimmer Biomet Zimmer Biomet

Hello,

I own a Zimmer Biomet that is covered by recall Z-2536-2019 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-2536-2019 (August 15, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2536-2019 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 83 mm Item # 195253

Recall notice