Zimmer Biomet recalls specific hip fracture nail models due to set screw malfunction. 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 advance or reverse from its original position. This could lead to improper fixation of the hip fracture, risking complications during healing.
The set screw in the nail fails to move properly from its starting position. This could result in the nail not securing the bone fragments correctly, potentially causing improper healing or requiring additional surgery.
Orthopedic surgeons and medical professionals who use these specific hip fracture nail models are affected. Patients receiving these implants during surgery are at risk if the set screw malfunctions.
Check for the model name 'Affixus Hip Fracture Nail Left 125' with dimensions 9 mm x 380 mm. The item number 814409380 is also associated with this recall.
Verify the model name, dimensions, and item number to confirm if your product is affected.
The recall applies to the surgical implants used by medical professionals. Patients receiving these implants during surgery are affected if the set screw malfunctions.
Check for the model name 'Affixus Hip Fracture Nail Left 125' with dimensions 9 mm x 380 mm and item number 814409380.
The recall does not specify a remedy, so contact Zimmer Biomet directly for further 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-3084-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3084-2018 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.
