Zimmer Biomet recalls Affixus Hip Fracture Nail Right 130 model with set screw that won't advance or reverse, potentially causing 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 due to a set screw that cannot advance or reverse properly. This could lead to improper bone fixation and complications during surgery.
The set screw in the nail fails to move forward or backward from its initial position. This prevents the nail from being properly secured in the bone, which could result in the nail becoming loose or failing during surgery.
Surgical patients who received this specific hip fracture nail model during procedures. Surgeons and medical staff using this product are most at risk of improper fixation.
Check for the model name 'Affixus Hip Fracture Nail Right 130' with dimensions 11 mm x 300 mm and item number 814511300. This product was sold in the U.S. under the specific item count of 558960.
Verify the model number and dimensions to confirm if the product is affected.
The recall indicates a potential issue with the set screw not advancing or reversing, which could lead to improper bone fixation during surgery. However, the hazard is not described as causing serious injury in normal use.
The recall does not specify a remedy, so no action is required beyond checking product details to confirm if it is affected.
Look for the model name 'Affixus Hip Fracture Nail Right 130' with dimensions 11 mm x 300 mm and item number 814511300.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-3123-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3123-2018 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.
