Zimmer Biomet XP-XP Tibial Tray - Interlok 69mm 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 69mm (Item #195754) because the locking bar may not fully engage, potentially causing improper fixation during surgery. This could lead to complications if the implant is not securely anchored.

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, potentially leading to complications like displacement or failure of the implant to function correctly.

Who’s affected

Orthopedic surgeons and medical professionals who use this specific surgical implant are likely affected. Patients receiving this implant during surgery are at risk if the locking bar fails to engage properly.

How to tell if you have this one

Check for the product name 'XP-XP Tibial Tray - Interlok 69mm' with Item #195754. Affected units have specific lot numbers listed in the recall: 590860, 560490, and other numbers provided in the record.

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 to confirm if your implant is affected.

✎ GovInfoNow

Questions people ask

What is the specific model of the recalled implant?

The recalled product is XP-XP Tibial Tray - Interlok 69mm with Item #195754.

How can I tell if my implant is affected?

Check for the product name 'XP-XP Tibial Tray - Interlok 69mm' with Item #195754 and specific lot numbers listed in the recall.

Is there a remedy for this recall?

The recall record states the remedy is null, meaning no specific action is required beyond checking if the product is affected.

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-2523-2019 — Zimmer Biomet Zimmer Biomet

Hello,

I own a Zimmer Biomet that is covered by recall Z-2523-2019 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-2523-2019 (August 15, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2523-2019 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 69 mm Item # 195754

Lower-risk recall