Zimmer Biomet recalls Affixus Hip Fracture Nail Left 130 (11mm x 360mm) due to set screw not advancing or reversing properly. Affected units may require replacement to prevent improper fixation.
The set screw is not able to advance or reverse from the original position in the nail.
Zimmer Biomet is recalling a specific hip fracture nail model because its set screw can't move correctly. This could lead to improper bone fixation and potential complications during healing.
The set screw in this hip fracture nail cannot advance or reverse from its original position. This may cause the nail to become improperly fixed in the bone, potentially leading to complications during healing.
Patients who received the Affixus Hip Fracture Nail Left 130 (11mm x 360mm) with item number 814611360 are affected. Surgeons and patients using this specific model are most at risk.
Check for the model name 'Affixus Hip Fracture Nail Left 130' with dimensions 11 mm x 360 mm and item number 814611360. The product was sold under the manufacturer's name Zimmer Biomet.
Reach out to Zimmer Biomet directly for guidance on the recall process and potential replacement options.
The recall indicates the set screw may not advance or reverse properly, which could lead to improper bone fixation. However, the hazard is described as low risk.
Check for the model name 'Affixus Hip Fracture Nail Left 130' with dimensions 11 mm x 360 mm and item number 814611360.
Contact Zimmer Biomet directly for guidance on the recall process and potential replacement options.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-3157-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3157-2018 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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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.
