Zimmer Biomet recalls Affixus Hip Fracture Nail Right 130 (13mm x 420mm) due to set screw not advancing or reversing properly. Affected units sold between 2006-2020; contact for remedy.
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 doesn't work correctly. This could lead to improper fixation of the hip fracture, risking complications during healing.
The set screw in this hip fracture nail cannot move forward or backward from its starting position. This means the nail might not stay securely in place during healing, potentially causing the fracture to shift or fail to heal properly.
Orthopedic surgeons and medical facilities using the Affixus Hip Fracture Nail Right 130 (13mm x 420mm) for hip fracture repairs. Patients receiving this specific implant are at risk if the set screw fails during surgery.
Check for the product name 'Affixus Hip Fracture Nail Right 130' with dimensions 13 mm x 420 mm. The item number 814513420 is also listed. Units were sold between 2006 and 2020.
Verify the product name, dimensions, and item number to confirm if your unit is affected.
The recall is for a set screw that doesn't advance or reverse properly, which could lead to improper fixation of the hip fracture. However, the hazard is not described as causing serious injury in normal use, so it's considered low risk.
Check for the product name 'Affixus Hip Fracture Nail Right 130' with dimensions 13 mm x 420 mm and item number 814513420. Units were sold between 2006 and 2020.
The recall record does not specify a remedy, so contact Zimmer Biomet directly for further instructions.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-3139-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3139-2018 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.
