Zimmer Biomet recalls left hip fracture nails with set screw issues that may not advance or reverse properly. Affected models include 130¿ 13 mm x : 814613340. Contact for remedy.
The set screw is not able to advance or reverse from the original position in the nail.
Zimmer Biomet is recalling left hip fracture nails that have a set screw which may not advance or reverse properly. This could lead to improper fixation of the hip fracture, potentially causing complications during healing.
The set screw in the nail may not advance or reverse from its original position. This could prevent the nail from being properly secured in the bone, leading to potential displacement or failure of the fixation during healing.
Patients who received the recalled hip fracture nail (model 130¿ 13 mm x 340 mm, item number 814613340) from Zimmer Biomet are affected. Surgeons and medical staff using this specific model during procedures are at higher risk.
Check for the model name '130¿ 13 mm x 340 mm' and item number 814613340 on the product packaging or label. The recall applies to specific hip fracture nails sold by Zimmer Biomet.
Identify the model number and item number on the product packaging or label.
This recall applies to specific Zimmer Biomet hip fracture nails with model 130¿ 13 mm x 340 mm and item number 814613340. Check your product details to confirm.
The recall record does not specify a remedy, so contact Zimmer Biomet directly for guidance.
Look for the model name '130¿ 13 mm x 340 mm' and item number 814613340 on the product packaging or label.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-3167-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3167-2018 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.
