Zimmer Biomet recalls Affixus Hip Fracture Nail Left 130 (11mm x 320mm) due to set screw not advancing or reversing properly. Affected units may require replacement.
The set screw is not able to advance or reverse from the original position in the nail.
Zimmer Biomet is recalling a specific hip fracture nail model because the set screw cannot move correctly. This could lead to improper fixation of the hip fracture, potentially causing complications during healing.
The set screw in the nail fails to advance or reverse from its original position. This means the nail may not hold securely in the bone, which could lead to improper fracture fixation and potential complications during healing.
Patients who received the Affixus Hip Fracture Nail Left 130 (11mm x :320mm) with item number 814611320 are affected. Surgeons and medical staff using this model during procedures are most at risk.
Check for the product name 'Affixus Hip Fracture Nail Left 130' with dimensions 11 mm x 320 mm and item number 814611320. The recall covers specific units sold under these identifiers.
Reach out to Zimmer Biomet directly to confirm if your specific unit is affected and to arrange for replacement.
The recall indicates a potential issue with the set screw not advancing or reversing properly, which could affect fracture fixation. However, the hazard is not described as causing serious injury in normal use.
Check for the product name 'Affixus Hip Fracture Nail Left 130' with dimensions 11 mm x 320 mm and item number 814611320.
Contact Zimmer Biomet directly to confirm if your unit is affected and to arrange for replacement.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-3155-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3155-2018 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.
