Zimmer Biomet recalls Affixus Hip Fracture Nails with set screw that cannot advance or reverse, posing a risk of improper fixation during hip fracture surgery.
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't move properly. This could lead to improper fixation of the hip fracture, potentially causing complications during surgery.
The set screw in the nail cannot advance or reverse from its original position. This means the nail may not stay securely in place during hip fracture surgery, potentially leading to improper fixation of the bone.
Surgical patients who received the Affixus Hip Fracture Nail 125 with item number 814311180. Surgeons and medical staff using this specific nail model are most at risk.
Check for the Affixus Hip Fracture Nail 125 (11 mm x 180 mm) with item number 814311180. This model was sold in specific batches between 2017 and 2020 as listed in the recall notice.
Verify the item number on the nail packaging to confirm if it matches 814311180.
The recall is for a set screw that cannot advance or reverse, which could lead to improper fixation during hip fracture surgery. However, the hazard is not described as causing serious injury in normal use.
Look for the Affixus Hip Fracture Nail 125 (11 mm x 180 mm) with item number 814311180. This model was sold in specific batches between 2017 and 2020.
The recall does not specify a remedy, so 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-3055-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3055-2018 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.
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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.
