Zimmer Biomet recalls Affixus Hip Fracture Nails 130 model with set screw that cannot advance or reverse, potentially causing improper fixation during hip fracture surgery.
The set screw is not able to advance or reverse from the original position in the nail.
Zimmer Biomet is recalling Affixus Hip Fracture Nails 130 (11 mm x 180 mm) because the set screw may not advance or reverse properly. This could lead to improper fixation of the hip fracture, risking complications during surgery.
The set screw in the nail cannot advance or reverse from its original position. This may cause the nail to become improperly fixed during hip fracture surgery, potentially leading to complications or the need for additional procedures.
Medical professionals who use these hip fracture nails during surgery are most at risk. Patients receiving this specific nail model may be affected if their surgery uses the recalled product.
Check for the model number 130 on the nail, which is 11 mm x 180 mm. The item number 814511180 is also associated with this recall. This product was sold from 2020 through 2023 based on the serial numbers listed.
Verify the model number (130) and item number (814511180) on the nail to confirm if it is recalled.
The set screw may not advance or reverse from its original position, which could lead to improper fixation during hip fracture surgery.
Look for the model number 130 on the nail, which is 11 mm x 180 mm, and item number 814511180.
Check the product details to confirm if it is recalled; if so, contact Zimmer Biomet 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-3120-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3120-2018 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.
