Zimmer Biomet recalls Affixus Hip Fracture Nails 125mm 9mm x 180mm (Item 814309180) due to set screw not advancing or reversing properly. This could affect surgical 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 may not advance or reverse from its original position. This could lead to improper surgical fixation if the nail is used.
The set screw in the nail may not move forward or backward from its starting position. This could cause the nail to become improperly fixed in the bone during surgery, potentially leading to complications.
Surgical patients who received the recalled Affixus Hip Fracture Nail 125mm 9mm x 180mm (Item 814309180) during procedures. Patients who have already had surgery with this model are most at risk.
Check for the Affixus Hip Fracture Nail 125mm 9mm x 180mm with Item Number 814309180. This model was sold in specific batches between 2017 and 2020 as listed in the product codes.
Verify the item number on the nail packaging or label to confirm if it matches 814309180.
This recall applies to the specific nail model used in procedures. If you received the Affixus Hip Fracture Nail 125mm 9mm x 180mm (Item 814309180), contact your surgeon to discuss potential risks.
Look for the item number 814309180 on the nail packaging or label. This model was sold in specific batches between 2017 and 2020.
The official recall does not specify a remedy. Check with your surgeon or healthcare provider for guidance on next steps.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-3047-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3047-2018 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.
