Zimmer Biomet Peg Recall: 22mm Peg Found in 10mm Units

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Contact the company & request your remedy

Recalling firmZimmer Biomet, Inc.56 E Bell Dr, N/A · 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 certain orthopedic pegs because a larger 22mm threaded peg was mistakenly included in some packages of the intended 10mm units. This could lead to improper bone fixation during surgery.

Why it’s dangerous

The recall involves a 22mm threaded peg being mistakenly included in packages of the smaller 10mm units. This larger peg could cause improper fixation of bone fragments during surgery, potentially leading to complications.

Who’s affected

Orthopedic surgeons and medical professionals who use Zimmer Biomet's Peg Fully Threaded, Locking 2.5mm x 10mm units for bone stabilization. Patients receiving these procedures are not directly affected.

How to tell if you have this one

Check the item number on the package: 131212610. The product is a Peg Fully Threaded, Locking 2.5mm x 10mm orthopedic device used for stabilization and fixation of small bone fragments.

Brand
Zimmer Biomet
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Package Contents
Inspect the package for a 22mm threaded peg that was mistakenly included in some 10mm units.

✎ GovInfoNow

Questions people ask

Why is this product being recalled?

A 22mm threaded peg was found in the package of a 10mm unit, which could cause improper fixation of bone fragments during surgery.

How can I tell if I have the recalled product?

Look for the item number 131212610 on the package. The product is a Peg Fully Threaded, Locking 2.5mm x 10mm orthopedic device.

What should I do if I have the recalled product?

Inspect the package for a 22mm threaded peg. If found, do not use the product and contact Zimmer Biomet 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-2965-2018 — Zimmer Biomet Zimmer Biomet

Hello,

I own a Zimmer Biomet that is covered by recall Z-2965-2018 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-2965-2018 (July 12, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2965-2018 to see it in context.
Plain-language summary written by qwen3:4b on August 20, 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 Peg Fully Threaded, Locking, 2.5mm x 10mm, Item Number 131212610 Orthopedic device used for stabilization and fixation

Lower-risk recall