Zimmer Biomet recalls Affixus Hip Fracture Nail 130 (13mm x 180mm) due to set screw not advancing or reversing properly. Affected units sold between 2020-2023; contact for remedy.
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 (13mm x 180mm) because the set screw can't move correctly. This could lead to improper fixation during hip fracture surgery, risking complications for patients.
The set screw in the nail cannot advance or reverse from its original position. This means the nail may not stay securely in place during surgery, potentially causing the implant to shift or fail.
Patients who received this specific hip fracture nail during surgery between 2020 and 2023 are affected. Surgeons using the product for hip fracture repairs are most at risk of complications.
Check for the product name 'Affixus Hip Fracture Nail 130' with dimensions 13 mm x 180 mm. The item number 814513180 is listed on the packaging. Units were sold between 2020 and 02/2023.
Reach out to Zimmer Biomet directly for instructions on how to handle the recalled product.
The recall states the set screw may not advance or reverse correctly, which could lead to improper fixation during surgery. This is a safety concern even with proper use.
Check for the product name 'Affixus Hip Fracture Nail 130' with dimensions 13 mm x 180 mm and item number 814513180 on the packaging or label.
The recall does not specify a stop-use instruction; the remedy is to contact the manufacturer for guidance.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-3132-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3132-2018 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.
