Zimmer Biomet recalls specific hip fracture nail models due to set screw failure. 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 can't move properly. This could lead to improper bone fixation during surgery, risking complications for patients.
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 surgery, potentially causing improper bone fixation and complications.
Patients who received the specific hip fracture nail model (125mm, 13mm x 260mm) from Zimmer Biomet. Surgeons and medical staff using these nails during procedures are most at risk.
Check for the model name 'Affixus Hip Fracture Nail Right 125' with dimensions 13 mm x 260 mm. The item number 814313260 is also associated with this recall.
Verify the model name, dimensions, and item number to confirm if your nail is affected.
The recall indicates the set screw may not advance or reverse properly, which could lead to improper bone fixation during surgery. However, the hazard is not described as causing serious injury in normal use.
The recall does not provide specific action steps for affected items. Check the product details to confirm if your nail is affected.
Look for the model name 'Affixus Hip Fracture Nail Right 125' with dimensions 13 mm x 260 mm and item number 814313260.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-3067-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3067-2018 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.
