Zimmer Biomet recalls Affixus Hip Fracture Nail Right 125 (9mm x 460mm) due to set screw not advancing or reversing properly. Affected units may not function correctly during hip fracture repair.
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 can't move properly. This could lead to improper fixation of the bone during surgery, potentially causing complications for patients.
The set screw in the nail cannot advance or reverse from its original position. This means the nail might not hold securely in the bone during hip fracture repair, which could lead to improper healing or complications.
Patients who received this specific hip fracture nail model during surgery are affected. Surgeons and medical staff using the product for hip fracture repairs are at risk if the set screw issue impacts surgical outcomes.
Check for the product name 'Affixus Hip Fracture Nail Right 125' with dimensions 9 mm x 460 mm. The item number 814309460 is also associated with this recall.
Verify the product name, dimensions, and item number to confirm if it matches the recalled model.
The recall indicates a potential issue with the set screw, but the product is not safe for use as it may not function correctly during hip fracture repair.
The recall does not specify a remedy, so contact Zimmer Biomet directly for guidance on next steps.
Look for the product name 'Affixus Hip Fracture Nail Right 125' with dimensions 9 mm x 460 mm and item number 814309460.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-3054-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3054-2018 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.
