Zimmer Biomet recalls hip fracture nail model 125 with set screw issues that may not advance or reverse properly. Affected units include item number 814411340.
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 may not advance or reverse from its original position. This could lead to improper fixation of the hip fracture, potentially causing complications during surgery or recovery.
The set screw in the nail may not move forward or backward from its starting position. This could prevent the nail from properly securing the hip fracture site, leading to potential complications during surgery or after the procedure.
Surgical patients who received the recalled hip fracture nail model 125 (11 mm x 34:0 mm) with item number 814411340. Surgeons and medical staff using this specific model during procedures are most at risk.
Check for the model name 'Affixus Hip Fracture Nail Left 125' with dimensions 11 mm x 340 mm and item number 814411340. The product was sold under the item number 814411340.
Verify the model name, dimensions, and item number to confirm if your nail is affected.
This recall applies to specific models with item number 814411340. Check your product details to see if you have the affected model.
The recall does not provide a remedy, so contact Zimmer Biomet directly for further instructions.
Look for the model name 'Affixus Hip Fracture Nail Left 125' with dimensions 11 mm x 340 mm and item number 814411340.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-3091-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3091-2018 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.
