Zimmer Biomet recalls Affixus Hip Fracture Nail Right 130 (11mm x 420mm) due to set screw not advancing or reversing. Affected units may need repair or replacement.
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 the set screw cannot move properly. This could lead to improper fixation of the hip fracture, risking complications during healing.
The set screw in the nail is designed to secure the implant in place. If it cannot advance or reverse from the original position, the nail may not hold securely, potentially causing the implant to shift during healing or movement.
Orthopedic surgeons and medical staff who use this specific hip fracture nail model during surgery. Patients receiving this implant are at risk if the set screw fails to function correctly.
Check for the model name 'Affixus Hip Fracture Nail Right 130', size 11 mm x 420 mm, and item number 814511420. The product was sold in specific quantities across different regions.
Verify the model name, size, and item number to confirm if your product is affected.
The recall is for a potential issue with the set screw not advancing or reversing, which could affect proper implant fixation. However, the hazard level is low risk as the remedy is not specified in the record.
The recall record does not specify a remedy, so no action is required beyond checking if your product matches the affected model.
Check for the model name 'Affixus Hip Fracture Nail Right 130', size 11 mm x 420 mm, and item number 814511420 as listed in the recall.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-3129-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3129-2018 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.
