Zimmer Biomet recalls Affixus Hip Fracture Nail Right 125mm model due to set screw not advancing or reversing properly. Affected units may require 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 doesn't work correctly. This could cause the nail to become loose or fail during use, potentially leading to complications after surgery.
The set screw in the nail cannot move forward or backward from its starting position. This means the nail might not stay securely in place during healing, which could lead to the nail becoming loose or failing after surgery.
Surgical patients who received the Affixus Hip Fracture Nail Right 125mm model (11 mm x 320 mm) from Zimmer Biomet. Patients who have had hip fracture surgery using this specific nail are most at risk.
Check for the model name 'Affixus Hip Fracture Nail Right 125mm' with dimensions 11 mm x 320 mm and item number 814311320. This specific nail was sold under the product code 900040.
Verify the model name, dimensions, and item number to confirm if your nail is affected.
The recall is for a set screw that doesn't advance or reverse properly, which could lead to the nail becoming loose. However, the hazard is not described as causing serious injury in normal use, so it's considered low risk.
Check for the model name 'Affixus Hip Fracture Nail Right 125mm' with dimensions 11 mm x 320 mm and item number 814311320. This specific nail was sold under the product code 900040.
The recall does not specify a remedy, so you should contact Zimmer Biomet directly for guidance on next steps.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-3058-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3058-2018 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.
