Zimmer Biomet recalls Affixus Hip Fracture Nail Right 125 model due to set screw not advancing or reversing properly. 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 correctly. This could lead to improper fixation of the hip fracture, potentially causing complications during healing.
The set screw in the nail fails to advance or reverse from its original position. This means the nail may not hold securely in place, which could lead to improper healing of the hip fracture.
Patients who received the Affixus Hip Fracture Nail Right 125 model (13 mm x 420 mm) from Zimmer Biomet. Surgeons and medical staff using this specific product are most at risk.
Check for the model name 'Affixus Hip Fracture Nail Right 125' with dimensions 13 mm x 420 mm. The item number is 814313420. This product was sold by Zimmer Biomet.
Reach out to Zimmer Biomet directly to confirm if your specific unit is affected and to get instructions for repair or replacement.
The set screw may not advance or reverse properly, which could lead to improper hip fracture fixation. However, the recall indicates it is a low-risk issue requiring monitoring.
Check for the model name 'Affixus Hip Fracture Nail Right 125' with dimensions 13 mm x 420 mm and item number 814313420.
Contact Zimmer Biomet directly to determine if your unit is affected and to get instructions for repair or replacement.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-3075-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3075-2018 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.
