Zimmer Biomet recalls Affixus Hip Fracture Nail Right 130mm 9mm x 360mm (item 814509360) due to set screw not advancing or reversing properly. Affected users should 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 can't move correctly. This could lead to improper fixation of the hip fracture, risking complications during healing.
The set screw in the nail cannot advance or reverse from its original position. This means the nail might not stay securely in place after surgery, potentially causing the hip fracture to shift or fail to heal properly.
Patients who received the Affixus Hip Fracture Nail Right 130mm 9mm x 360mm (item 814509360) from Zimmer Biomet. Surgeons and medical staff using this model during procedures are most at risk.
Check for the Affixus Hip Fracture Nail Right 130mm 9mm x 360mm with item number 814509360 or 813470. This product was sold by Zimmer Biomet.
Reach out to Zimmer Biomet for instructions on how to handle the recalled nail.
The recall is for a set screw that may not advance or reverse properly, which could affect hip fracture fixation. However, the hazard level is low risk as the remedy is contact-based without immediate stop-use instructions.
Check for the Affixus Hip Fracture Nail Right 130mm 9mm x 360mm with item numbers 814509360 or 813470.
Contact Zimmer Biomet for instructions on how to handle the recalled nail.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-3114-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3114-2018 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.
