Zimmer Biomet recalls hip fracture nails with set screw that won't advance or reverse. Affected models may need repair or replacement to prevent improper fixation.
The set screw is not able to advance or reverse from the original position in the nail.
Zimmer Biomet is recalling hip fracture nails that have a set screw which won: not advance or reverse from the original position. This could lead to improper fixation of the hip fracture. Affected users should contact the company for guidance.
The set screw in the nail cannot move forward or backward from its starting position. This may cause the nail to become improperly fixed in the bone, potentially leading to complications during healing.
Patients who received the Affixus Hip Fracture Nail Right 130 model (11 mm x 260 mm) with item number 814511260. Those at highest risk are individuals who have undergone hip fracture surgery using this specific nail.
Check for the model name 'Affixus Hip Fracture Nail Right 130', size 11 mm x 260 mm, and item number 814511260. The product was sold under the brand Zimmer Biomet.
Reach out to Zimmer Biomet directly for instructions on how to handle the recalled nail.
The recall indicates a set screw that won't advance or reverse, which could lead to improper fixation. However, the hazard level is low risk as the remedy involves contacting the manufacturer for guidance.
Check for the model name 'Affixus Hip Fracture Nail Right 130', size 11 mm x 260 mm, and item number 814511260.
Contact Zimmer Biomet directly 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-3121-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3121-2018 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.
