Zimmer Biomet recalls Affixus Hip Fracture Nail Right 125 (13mm x 180mm) due to set screw not advancing or reversing properly. Affected units sold between 2019-2020; consumers should contact manufacturer 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 its set screw can't move properly. This could lead to improper fixation of the hip fracture, risking complications during healing.
The set screw in the nail cannot advance or reverse from its original position. This means the nail may not stay securely in place after surgery, potentially causing the hip fracture to shift or fail to heal properly.
Patients who received the Affixus Hip Fracture Nail Right 125 (13mm x 180mm) from Zimmer Biomet. Surgeons and medical staff using this model for hip fracture repairs are most at risk.
Check for the model name 'Affixus Hip Fracture Nail Right 125' with dimensions 13 mm x 180 mm. The item number 814313180 is also associated with this recall. Units were sold between 2019 and 2020.
Reach out to Zimmer Biomet directly for specific instructions on how to handle the recalled item.
The recall states the set screw cannot advance or reverse properly, which could lead to improper fixation. However, the hazard is not described as causing immediate injury in normal use.
Check for the model name 'Affixus Hip Fracture Nail Right 125' with dimensions 13 mm x 180 mm and item number 814313180. Units were sold between 2019 and 2020.
The recall does not specify a remedy, so contact Zimmer Biomet directly for instructions.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-3066-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3066-2018 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.
