Zimmer Biomet recalls Affixus Hip Fracture Nail Left 125mm (Item 814409260) due to set screw not advancing or reversing properly. Affected patients should contact for guidance.
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 doesn't work correctly. This could lead to improper fixation of the hip fracture, risking complications during healing.
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, potentially causing the hip fracture to shift or fail to heal properly.
Patients who received the Affixus Hip Fracture Nail Left 125mm (9 mm x 260 mm) with item number 814409260 are affected. Surgeons and medical staff using this product for hip fracture repairs are most at risk.
Check for the product name 'Affixus Hip Fracture Nail Left 125mm', size 9 mm x 260 mm, and item number 814409260. This product was sold under the item code 971030.
Reach out to Zimmer Biomet directly for guidance on next steps.
The set screw may not advance or reverse properly, which could lead to improper hip fracture fixation. However, the recall indicates it's a low-risk issue requiring medical guidance.
Check for the product name 'Affixus Hip Fracture Nail Left 125mm', size 9 mm x 260 mm, and item number 814409260.
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-3078-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3078-2018 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.