Zimmer Bi: XP-XP Tibial Tray Interlok 87mm Recall - Locking Bar Not Fully Engaging

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

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Zimmer Biomet is recalling XP-XP Tibial Tray Interlok 87mm models with specific lot numbers 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 cause the implant to become loose during surgery. This might lead to improper fixation of the bone, potentially causing complications or requiring additional surgery.

Who’s affected

Surgical patients and medical professionals using Zimmer Biomet's XP-XP Tibial Tray Interlok 87mm implants with the listed lot numbers. Patients undergoing orthopedic surgery are most at risk.

How to tell if you have this one

Check the product label for the lot numbers: 790970, 984810, 984820, 202000R, 664250R, 664280R, 885800, 716010, 873630, 903460, 960480, 960500, 201990, 202000, 664250, 664280, 400690, 394670, 394710, 293220, 183680, 394330.

Brand
Zimmer Biomet
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Label
Look for the lot numbers listed in the recall notice to determine if your item is affected.

✎ GovInfoNow

Questions people ask

What is the specific model of the recalled product?

The recalled product is Zimmer Biomet's XP-XP Tibial Tray Interlok 87mm with Item #195760.

How can I tell if my product is affected by this recall?

What should I do if I have the recalled product?

The recall notice does not specify a remedy, so contact Zimmer Biomet directly for further instructions.

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-2517-2019 — Zimmer Biomet Zimmer Biomet

Hello,

I own a Zimmer Biomet that is covered by recall Z-2517-2019 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-2517-2019 (August 15, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2517-2019 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 XP-XP Tibial Tray - Interlok 87 mm Item # 195760

Recall notice