Zimmer Biomet Affixus Hip Fracture Nail Left 125mm Recall: 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 Affixus Hip Fracture Nails Left 125mm (Item 814409440) because the set screw can't move properly. 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 place, which could lead to improper healing of the hip fracture.

Who’s affected

Patients who received the Affixus Hip Fracture Nail Left 125mm (Item 814409440) from Zimmer Biomet are affected. Orthopedic surgeons and patients using this specific implant are most at risk.

How to tell if you have this one

Check for the Affixus Hip Fracture Nail Left 125mm with Item Number 814409440. The product was sold under the item numbers 814409440 and 503610 900270.

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 to confirm if your specific implant is affected and get instructions for replacement.

✎ GovInfoNow

Questions people ask

Is this recall affecting my hip surgery implant?

This recall applies to Affixus Hip Fracture Nails Left 125mm with Item Number 814409440. If you have this specific model, contact Zimmer Biomet for guidance.

How do I know if my implant is affected?

Check the item number on your implant; affected units have Item Number 814409440 or 503610 900270.

What should I do if I have this implant?

Contact Zimmer Biomet directly to determine if your implant is affected and to get instructions for replacement.

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-3087-2018 — Zimmer Biomet Zimmer Biomet

Hello,

I own a Zimmer Biomet that is covered by recall Z-3087-2018 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-3087-2018 (July 17, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3087-2018 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¿ 9 mm x 440 mm, Item Number: 814409440

Lower-risk recall