Zimmer Biomet recalls Affixus Hip Fracture Nail Right 125 model due to set screw not advancing or reversing properly. Affected units may require repair or 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 the set screw cannot move forward or backward as intended. This could prevent the nail from staying securely in place during surgery, potentially causing complications.
The set screw in the nail is designed to move in and out to secure the implant. If it cannot advance or reverse, the nail may not stay properly positioned during surgery, which could lead to complications like displacement or improper healing.
Surgical teams using the Affixus Hip Fracture Nail Right 125 model for hip fracture repairs are affected. Patients undergoing surgery with this specific nail are at risk of improper fixation.
Check for the model name 'Affixus Hip Fracture Nail Right 125' with dimensions 13 mm x 360 mm and item number 814313360. The product was sold under the manufacturer's name Zimmer Biomet.
Reach out to Zimmer Biomet directly for guidance on the recall and potential remedies.
The recall indicates the set screw may not advance or reverse properly, which could affect surgical fixation. However, the hazard level is low risk as the remedy involves contacting the manufacturer for guidance.
Check for the model name 'Affixus Hip Fracture Nail Right 125' with dimensions 13 mm x 360 mm and item number 814313360.
Contact Zimmer Biomet directly for guidance on the recall and potential remedies.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-3072-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3072-2018 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.
