Zimmer Biomet recalls specific hip fracture nail models due to set screw failure. Affected items may not advance or reverse properly, 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 certain hip fracture nail models because the set screw cannot properly advance or reverse. 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 starting position. This prevents the nail from securely anchoring to bone, which could cause the nail to loosen during surgery or after implantation.
Surgical teams using the affected hip fracture nail models during procedures. Patients receiving these nails are at risk of improper fixation.
Check for the model name 'Affixus Hip Fracture Nail Right 125' with dimensions 13 mm x 320 mm. The item number 814313320 is also associated with this recall.
Verify the model name, dimensions, and item number to confirm if your nail is affected.
The recall indicates the set screw may not advance or reverse properly, which could lead to improper bone fixation. However, the hazard is described as a potential issue during use, not an immediate risk to safety.
The recall does not specify a remedy, so you should check the product details to confirm if it's affected and contact Zimmer Biomet for further guidance.
Look for the model name 'Affixus Hip Fracture Nail Right 125' with dimensions 13 mm x 320 mm and item number 814313320.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-3070-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3070-2018 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.
