Zimmer Biomet recalls Affixus Hip Fracture Nail Left 125 (11mm x 440mm) due to set screw not advancing or reversing properly. Affected units may cause improper fixation.
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 cannot move correctly. This could lead to improper bone fixation and potential complications after surgery.
The set screw in the nail fails to advance or reverse from its original position. This means the nail may not secure the bone fragments properly during surgery, potentially leading to improper healing or complications.
Surgical patients who received the Affixus Hip Fracture Nail Left 125 (11mm x 440mm) with item number 814411440. Patients who have had hip fracture surgery using this model are most at risk.
Check for the product name 'Affixus Hip Fracture Nail Left 125' with dimensions 11 mm x 440 mm and item number 814411440. This model was sold in specific batches identified by the numbers 151870, 155110, 646620, 960600, 646630, and 646640.
Identify the product name, dimensions, 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 is described as low risk.
Check for the product name 'Affixus Hip Fracture Nail Left 125' with dimensions 11 mm x 440 mm and item number 814411440. Affected units were sold in specific batches identified by the numbers 151870, 155110, 646620, 960600, 646630, and 646640.
The recall does not specify a remedy, so you should check with Zimmer Biomet directly for guidance.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-3096-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3096-2018 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.
