Zimmer Biomet XP-XP Tibial Tray - Interlok 75mm Recall: Locking bar may not engage properly

Take action

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 75mm (Item #195757) because the locking bar might 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 result in the implant not staying securely in place during surgery. This might cause improper fixation, leading to potential complications like instability or misalignment of the knee joint.

Who’s affected

Patients who have undergone knee surgery using this specific implant model are most at risk. The recall affects certain lot numbers of the XP-XP Tibial Tray - Interlok 75mm.

How to tell if you have this one

Check the product label for the model name 'XP-XP Tibial Tray - Interlok 75mm' and item number 195757. Affected units have specific lot numbers listed in the recall notice.

Brand
Zimmer Biomet
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Contact Manufacturer
Reach out to Zimmer Biomet directly for assistance with the recall and to determine if your specific unit is affected.

✎ GovInfoNow

Questions people ask

What is the specific model being recalled?

The XP-XP Tibial Tray - Interlok 75mm (Item #195757) is being recalled.

How can I check if my implant is affected?

Check the product label for the model name and item number 195757. Affected units have specific lot numbers listed in the recall notice.

What should I do if I have this implant?

Contact Zimmer Biomet directly for assistance with the recall and to determine if your specific unit 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-2520-2019 — Zimmer Biomet Zimmer Biomet

Hello,

I own a Zimmer Biomet that is covered by recall Z-2520-2019 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.

Similar recalls

From people who’ve dealt with this

Experiences, tips, and questions from readers. Every comment is reviewed before it appears.

No comments yet — be the first to share your experience.

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-2520-2019 (August 15, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2520-2019 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-XP Tibial Tray - Interlok 75 mm Item # 195757

Recall notice