Zimmer Bi: XP-CR Tibial Tray - Porous Plasma 91mm Recall Due to Locking Bar Issue

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Contact the company & request your remedy

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 XP-CR Tibial Tray - Por:ous Plasma 91mm implants (Item #195291) because the locking bar may not engage properly. This could lead to improper fixation during surgery, potentially causing complications for patients.

Why it’s dangerous

The locking bar may not fully engage, which could result in the implant not staying securely in place during surgery. This might cause improper fixation and potential complications for the patient.

Who’s affected

Orthopedic surgeons and patients who received the recalled XP-CR Tibial Tray - Porous Plasma 91mm implants (Item #195291) with Lot Numbers 149710 or 615950. Surgeons using these implants during procedures are most at risk.

How to tell if you have this one

Check if your implant has the model name 'XP-CR Tibial Tray - Porous Plasma 91mm', item number 195291, and lot numbers 149710 or 615950.

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, item number, and lot numbers to confirm if it matches the recalled items.

✎ GovInfoNow

Questions people ask

Is this recall affecting my surgery?

The recall applies to implants used in surgery. If you received the recalled model, contact Zimmer Biomet for guidance.

How can I confirm if my implant is recalled?

Check if your implant is labeled as 'XP-CR Tibial Tray - Porous Plasma 91mm' with item number 195291 and lot numbers 149710 or 615950.

What should I do if I have the recalled implant?

The recall 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-2515-2019 — Zimmer Biomet Zimmer Biomet

Hello,

I own a Zimmer Biomet that is covered by recall Z-2515-2019 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-2515-2019 (August 15, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2515-2019 to see it in context.
Plain-language summary written by qwen3:4b on August 10, 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 - Porous Plasma 91 mm Item # 195291

Lower-risk recall