Zimmer Biomet recalls Affixus Hip Fracture Nail Right 130 model due to set screw not advancing or reversing properly. Affected units may need 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 advance or reverse from its original position. This could prevent proper fixation of the hip fracture, potentially leading to complications during surgery or recovery.
The set screw in the nail fails to move forward or backward from its starting position. This could cause the nail to become loose or misaligned during surgery, potentially leading to improper healing of the hip fracture.
Surgical patients who received the Affixus Hip Fracture Nail Right 130 model (13 mm x 3:40 mm) with item number 814513340. Orthopedic surgeons and hospitals using this model are most at risk.
Check for the model name 'Affixus Hip Fracture Nail Right 130', size 13 mm x 340 mm, and item number 814513340. The product was sold under the item code 017700.
Verify the model name, size, and item number to confirm if your product is affected.
The recall is for a potential issue with the set screw not advancing or reversing, which could affect surgical fixation. However, the hazard level is low risk as the remedy is not specified and the issue may not cause serious injury in normal use.
The recall record does not specify a remedy, so there is no action required beyond checking if your product matches the description.
Check for the model name 'Affixus Hip Fracture Nail Right 130', size 13 mm x 340 mm, and item number 814513340. The product was sold under the item code 017700.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-3136-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3136-2018 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.
