Zimmer Biomet XP- CR Tibial Tray- Interlok 59mm 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- CR Tibial Tray- Interlok 59mm implants because the locking bar might not engage properly. This could lead to improper surgical alignment, potentially causing complications for patients during joint replacement procedures.

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 alignment of the joint, leading to potential complications after the procedure.

Who’s affected

Orthopedic surgeons and patients who have received the XP- CR Tibial Tray- Interlok 59mm implant (Item #195268) during surgery. Patients who have had the implant are at risk of improper alignment.

How to tell if you have this one

Check if your implant has the model name 'XP- CR Tibial Tray- Interlok 59mm' and item number 195268. Lot numbers include 004960, 262370, 130580, 004970, 130630, 130550, 130610, 130560, 130570, 004950, 130590, 279210.

Brand
Zimmer Biomet
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Implant Details
Review your implant's model name, item number, and lot numbers to confirm if it matches the recalled product.

✎ GovInfoNow

Questions people ask

Is this recall affecting me?

If you have the XP- CR Tibial Tray- Interlok 59mm implant (Item #195268) with the listed lot numbers, this recall applies to you.

What should I do if I have this implant?

The recall record does not specify a remedy, so contact Zimmer Biomet directly for guidance.

How can I verify if my implant is recalled?

Check the model name, item number, and lot numbers listed in the recall notice.

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-2503-2019 — Zimmer Biomet Zimmer Biomet

Hello,

I own a Zimmer Biomet that is covered by recall Z-2503-2019 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-2503-2019 (August 15, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2503-2019 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- CR Tibial Tray- Interlok 59mm Item # 195268

Recall notice