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

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Contact the company & request your remedy

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 63mm implants (Item #195751) because the locking bar might not engage properly during surgery. This could cause improper fixation of the implant, potentially leading to complications for patients.

Why it’s dangerous

The locking bar may not fully engage during surgery, which could result in the implant not being securely fixed to the bone. This might cause the implant to shift or become unstable after surgery, potentially leading to complications.

Who’s affected

Orthopedic surgeons and their patients who have received the recalled XP-XP Tibial Tray - Interlok 63mm implants (Item #195751) with specific lot numbers. Patients who have had surgery using this implant are most at risk.

How to tell if you have this one

Check the product label for the item number 195751 and lot numbers listed in the recall (e.g., 522520, 571140, 589700, etc.). This implant is used in orthopedic surgeries for knee replacements.

Brand
Zimmer Biomet
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Label
Look for the item number 195751 and lot numbers such as 522520, 571140, or 589700 on the implant packaging or label.

✎ GovInfoNow

Questions people ask

What is the specific model of the implant being recalled?

The recalled model is the XP-XP Tibial Tray - Interlok 63mm (Item #195751).

What lot numbers are affected?

Affected lot numbers include 522520, 571140, 589700, 758150, 028960, 028980, 043970, and many others as listed in the recall.

Is there a remedy for this recall?

The recall record states that no remedy is provided (remedy is null).

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-2526-2019 — Zimmer Biomet Zimmer Biomet

Hello,

I own a Zimmer Biomet that is covered by recall Z-2526-2019 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-2526-2019 (August 15, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2526-2019 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 63 mm Item # 195751

Lower-risk recall