Zimmer Biomet recalls Affixus Hip Fracture Nails 130 with set screw issues that may not advance or reverse properly. Affected units include specific item numbers sold between 2014-2020.
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 (9 mm x 180 mm) because the set screw may not advance or reverse from its original position. This could lead to improper fixation of the hip fracture, risking complications during surgery or recovery.
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, potentially leading to complications during surgery or after the procedure.
Patients who received the Affixus Hip Fracture Nail 130 (item number 814509180) for hip fracture treatment are affected. Surgeons and medical staff using this specific nail during procedures are at risk.
Check for the item number 814509180 on the nail packaging or label. The product was sold between 2014 and 2020 under the Affixus Hip Fracture Nail 130 (9 mm x 180 mm) name.
Look for the item number 814509180 on the nail packaging or label to confirm if it is affected.
The recall is for a set screw that may not advance or reverse properly, which could lead to improper fixation of the hip fracture. However, the hazard is not described as causing serious injury in normal use, so it is considered low risk.
Check for the item number 814509180 on the nail packaging or label. The product was sold between 2014 and 2020.
The recall does not specify a remedy, so no action is required. However, you should check with your surgeon or healthcare provider if you have concerns about the product.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-3108-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3108-2018 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.
