Zimmer Biomet recalls Affixus Hip Fracture Nail Right 130 model with set screw that won't advance or reverse. Consumers should contact 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 due to a set screw that cannot advance or reverse from its original position. This issue could prevent proper fixation of the nail, potentially affecting surgical outcomes.
The set screw in the nail cannot move forward or backward from its starting position. This may prevent the nail from holding securely in place during surgery, which could lead to improper healing or complications.
Medical professionals who use this specific hip fracture nail model during surgery are affected. Patients receiving this implant are at risk if the nail fails to secure properly.
Check for the model name 'Affixus Hip Fracture Nail Right 130' with dimensions 11 mm x 440 mm and item number 814511440. This product was sold by Zimmer Biomet.
Reach out to Zimmer Biomet directly for specific recall instructions and assistance.
The set screw may not advance or reverse, which could affect surgical fixation. However, the recall does not specify immediate injury risk.
Look for the model name 'Affixus Hip Fracture Nail Right 130' with dimensions 11 mm x 440 mm and item number 814511440.
Contact Zimmer Biomet directly for specific recall instructions and 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-3130-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3130-2018 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.
