Zimmer Biomet recalls Affixus Hip Fracture Nail Right 125 (11mm x 400mm) due to set screw not advancing or reversing. Affected units have item number 814311400. Consumers should contact Zimmer Biomet for details.
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 cannot properly advance or reverse. This could lead to improper fixation of the hip fracture, risking complications during surgery or recovery.
The set screw in the nail fails to move forward or backward from its starting position. This could prevent the nail from securely fixing the hip fracture, potentially causing the implant to shift during surgery or after the procedure.
Surgical patients who received the Affixus Hip Fracture Nail Right 125 (11mm x 400mm) with item number 814311400. Surgeons and medical staff using this specific implant are most at risk.
Check for the product name 'Affixus Hip Fracture Nail Right 125' with dimensions 11 mm x 400 mm and item number 814311400. This model was sold with specific serial numbers listed in the recall notice.
Reach out to Zimmer Biomet directly for specific instructions on how to report the product and receive any necessary assistance.
The recall states the set screw may not advance or reverse, which could lead to improper fixation of the hip fracture. However, the hazard is not described as causing immediate serious injury in normal use.
Look for the product name 'Affixus Hip Fracture Nail Right 125' with dimensions 11 mm x 400 mm and item number 814311400. Check the serial numbers listed in the recall notice.
Contact Zimmer Biomet directly for specific instructions on how to report the product and receive any necessary assistance.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-3062-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3062-2018 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.
