Zimmer Biomet recalls specific hip fracture nails due to set screw not advancing or reversing properly. Affected models may require replacement to prevent improper fixation.
The set screw is not able to advance or reverse from the original position in the nail.
Zimmer Biomet is recalling hip fracture nails that have a set screw which cannot advance or reverse from its original position. This could lead to improper fixation of the hip fracture, potentially causing complications during healing.
The set screw in the nail cannot move forward or backward from its starting position. This means the nail may not secure properly to the bone, increasing the risk of the implant shifting or failing during healing.
Orthopedic surgeons and medical professionals who use the Affixus Hip Fracture Nail Right 125 model for hip fracture repairs. Patients receiving this specific implant are at risk if the set screw fails to function correctly.
Check for the Affixus Hip Fracture Nail Right 125 model with dimensions 11 mm x 300 mm and item number 814311300. This product was sold in specific quantities and may be used in hip fracture surgeries.
Verify the model number and dimensions to confirm if your nail is affected.
The recall is for a potential issue with the set screw not advancing or reversing, which could affect proper fixation. However, the hazard level is low risk as the remedy is not specified and the issue may not cause serious injury in all cases.
The recall record does not specify a remedy, so no action is required beyond checking if your product matches the description.
Check for the Affixus Hip Fracture Nail Right 125 model with dimensions 11 mm x 300 mm and item number 814311300.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-3057-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3057-2018 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.
