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 the nail not securing bones properly during surgery, potentially causing improper healing or requiring additional procedures.
Surgical patients who received the specific hip fracture nail model (125mm, 11mm x 360mm) with item number 814411360. Patients who have had the procedure using this model are most at risk.
Check for the model name 'Affixus Hip Fracture Nail Left 125mm 11 mm x 360 mm' and item number 814411360. The product was sold in specific quantities across multiple locations.
Verify the model name and item number to confirm if your nail is affected.
The recall indicates a potential issue with the set screw not advancing or reversing properly, which could affect bone fixation. However, the hazard level is low risk as the remedy is not specified and no immediate action is required.
The official recall record does not specify a remedy, so no action is required at this time. Check product details to confirm if you have the affected model.
Look for the model name 'Affixus Hip Fracture Nail Left 125mm 11 mm x 360 mm' and item number 814411360. The product was sold in specific quantities across multiple locations.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-3092-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3092-2018 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.
