Zimmer Biomet recalls left hip fracture nails with set screw issues that may not advance or reverse properly. Affected models include 125mm x 280mm, item 814: 559130. No remedy specified in recall notice.
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 result in the nail not being properly secured to the bone, which might lead to improper healing or complications during recovery.
Orthopedic surgeons and medical professionals who use Zimmer Biomet's Affixus Hip Fracture Nails for left hip fractures. The risk is low as the issue affects a specific component but does not cause immediate harm.
Check for the model number 814413280 on the nail packaging or label. The affected product is a left hip fracture nail with dimensions 13 mm x 280 mm, sold under the item number 559130.
Verify the model number and dimensions on the nail to confirm if it matches the recalled item.
The recall notice does not specify any remedy or fix for this issue.
Check for the model number 814413280 and dimensions 13 mm x 280 mm on the nail packaging or label.
The set screw may not advance or reverse properly, which could lead to improper fixation of the hip fracture, but the recall indicates this is a low-risk issue.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-3099-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3099-2018 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.