Zimmer Biomet recalls specific hip fracture nail models due to set screw failure. Affected items may not advance or reverse properly, potentially causing improper fixation.
The set screw is not able to advance or reverse from the original position in the nail.
Zimmer Biomet is recalling certain hip fracture nail models because the set screw can't move correctly. This could lead to improper bone fixation and complications during healing.
The set screw in the nail cannot advance or reverse from its original position. This may cause improper bone fixation, potentially leading to complications during healing or surgery.
Orthopedic surgeons and medical professionals using the Affixus Hip Fracture Nail Right 130 model. Patients receiving this specific implant are at risk if the set screw fails during surgery.
Check for the model name 'Affixus Hip Fracture Nail Right 130' with dimensions 9 mm x 460 mm. The item number is 814509460. This product was sold starting in 2019.
Verify the model name, dimensions, and item number to confirm if your product is affected.
The recall indicates a potential issue with the set screw, but the product is not unsafe for normal use. Affected items may not function correctly.
The recall does not specify a remedy, so contact Zimmer Biomet directly for guidance.
Check for the model name 'Affixus Hip Fracture Nail Right 130', dimensions 9 mm x 460 mm, and item number 814509460.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-3119-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3119-2018 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.