Zimmer Biomet Affixus Hip Fracture Nail Left 125 Recalls: Set Screw Malfunction

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Recalling firmZimmer Biomet, Inc.56 E Bell Dr, N/A · Warsaw, IN 46582-6989

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Zimmer Biomet is recalling a specific hip fracture nail model because its set screw doesn't move correctly. This could lead to improper fixation of the hip fracture, potentially causing complications during healing.

Why it’s dangerous

The set screw in the nail cannot advance or reverse from its original position. This means the nail might not hold securely in the bone, which could lead to the implant shifting or failing during healing.

Who’s affected

Orthopedic surgeons and medical professionals who use this specific hip fracture nail model during surgery. Patients who have received this implant are at risk of improper healing.

How to tell if you have this one

Check for the product name 'Affixus Hip Fracture Nail Left 125' with dimensions 13 mm x 260 mm. The item number is 814413260 or 814090.

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 guidance on next steps.

✎ GovInfoNow

Questions people ask

Is this recall affecting patients who have already had the surgery?

The recall does not specify if patients who have received the implant are affected. Zimmer Biomet has not provided details on this.

How can I check if my hip fracture nail is affected?

Check the product name, dimensions (13 mm x 260 mm), and item numbers (814413260 or 814090) on your device.

What should I do if I have this nail?

The recall does not specify a remedy. 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-3098-2018 — Zimmer Biomet Zimmer Biomet

Hello,

I own a Zimmer Biomet that is covered by recall Z-3098-2018 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-3098-2018 (July 17, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3098-2018 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 Affixus¿ Hip Fracture Nail Left 125¿ 13 mm x 260 mm, Item Number: 814413260

Lower-risk recall