Zimmer Biomet recalls Affixus Hip Fracture Nail Right 130 (11mm x 400mm) due to set screw not advancing or reversing properly. Affected units have item number 814511400. Consumers should contact Zimmer Biomet for details.
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 may not advance or reverse correctly. This could lead to improper fixation of the hip fracture, risking complications during surgery or recovery.
The set screw in the nail may not move forward or backward from its starting position. This could cause the nail to become improperly secured during hip fracture repair, potentially leading to complications like displacement or failure of the implant.
Surgical patients who received the Affixus Hip Fracture Nail Right 130 (11mm x 400mm) with item number 814511400. Surgeons and medical staff using this specific implant are most at risk.
Check if your hip fracture nail has the model name 'Affixus Right 130' and dimensions 11 mm x 400 mm. The item number 814511400 is also listed on the product.
Reach out to Zimmer Biomet directly for specific instructions on how to handle the recalled product.
The recall indicates a potential issue with the set screw, but the product is not considered immediately dangerous. Patients should follow the manufacturer's guidance.
Check for the model name 'Affixus Right 130', dimensions 11 mm x 400 mm, and item number 814511400 on the product.
Contact Zimmer Biomet directly for specific instructions on handling the recalled product.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-3128-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3128-2018 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.
