Zimmer Biomet XP-XP Tibial Tray - Interlok 91mm 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 91mm (Item #195761) because the locking bar might not engage fully during surgery. This could lead to improper alignment of the implant, potentially causing complications for patients.

Why it’s dangerous

The locking bar may not engage fully during surgery, which can cause improper alignment of the implant. This might lead to complications such as misalignment or instability of the joint, potentially affecting the surgical outcome.

Who’s affected

Orthopedic surgeons and their patients who have received the XP-XP Tibial Tray - Interlok 91mm (Item #195761) with specific lot numbers from 2020 to 2020. Patients are at risk if the implant does not align correctly during surgery.

How to tell if you have this one

Check the product label for the item number 195761 and lot numbers listed: 183700, 790980, 202030, 202020, 202010, 986220, 986240, 986240R, 396520, 986230, 394870, 394840, 833310, 394860, 903470, 508690, 701050, 701050R.

Brand
Zimmer Biomet
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Label
Look for item number 195761 and the specific lot numbers listed in the recall notice.

✎ GovInfoNow

Questions people ask

What is the specific model of the recalled product?

The recalled product is the XP-XP Tibial Tray - Interlok 91mm with item number 195761.

What lot numbers are affected?

Affected lot numbers include 183700, 790980, 202030, 202020, 202010, 986220, 986240, 986240R, 396520, 986230, 394870, 394840, 833310, 394860, 903470, 508690, 701050, 701050R.

Is there a remedy for this recall?

The recall notice does not specify a remedy.

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-2516-2019 — Zimmer Biomet Zimmer Biomet

Hello,

I own a Zimmer Biomet that is covered by recall Z-2516-2019 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-2516-2019 (August 15, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2516-2019 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 91mm Item # 195761

Lower-risk recall