Zimmer Biomet recalls specific hip fracture nail models due to set screw malfunction. Affected items may not advance or reverse properly, potentially causing improper fixation.
The set screw is not able to advance or reverse from the original position in the nail.
Zimmer Biomet is recalling certain hip fracture nail models because the set screw cannot properly advance or reverse. This could lead to improper bone fixation and increased risk of complications after surgery.
The set screw in the nail fails to move correctly from its original position. This could result in improper bone fixation during hip fracture repair, potentially causing complications like displacement or instability.
Surgical patients who received the recalled hip fracture nail model during procedures. Patients using the product for medical purposes are most at risk.
Check for the product name 'Affixus Hip Fracture Nail Left 130' with dimensions 9 mm x 280 mm. The item number 814609280 is also associated with this recall.
Verify the product name, dimensions, and item number to confirm if your nail is affected.
The recall indicates a potential issue with the set screw, but the risk is low as it does not cause immediate harm in normal use.
Check for the product name 'Affixus Hip Fracture Nail Left 130' with dimensions 9 mm x 280 mm and item number 814609280.
The recall does not specify a remedy, so contact Zimmer Biomet directly for guidance.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-3147-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3147-2018 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.