Zimmer Biomet recalls Affixus Hip Fracture Nail Right 125mm model due to set screw not advancing or reversing properly. Affected items may require replacement.
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 doesn't work correctly. This could prevent proper fixation of the hip fracture, potentially causing complications after surgery.
The set screw in the nail cannot move forward or backward from its starting position. This means the nail might not stay securely in place after surgery, which could lead to improper healing or complications.
Surgical patients who received this specific hip fracture nail model during surgery are affected. Patients who have had the procedure are most at risk.
Check for the model name 'Affixus Hip Fracture Nail Right 125mm' with item number 814313280. The product was sold under the item numbers 053750 and 813300.
Reach out to Zimmer Biomet directly to confirm if your specific item is affected and get instructions for replacement.
The recall is for a potential issue with the set screw not advancing or reversing, which could affect proper fixation after surgery. However, the hazard level is low risk as the remedy does not require immediate stop-use.
Check for the model name 'Affixus Hip Fracture Nail Right 125mm' with item number 814313280 or the item numbers 053750 and 813300.
Contact Zimmer Biomet directly to confirm if your specific item is affected and get instructions for replacement.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-3068-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3068-2018 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.
