Zimmer Biomet recalls left hip fracture nails with set screw issues that may not advance or reverse properly, posing potential fixation risks.
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 from its original position. This could lead to improper fixation of the hip fracture, risking complications during recovery.
The set screw in the nail may not advance or reverse from its original position, which could cause the nail to become loose or fail to hold properly. This might lead to improper fixation of the hip fracture, potentially causing pain, instability, or complications during healing.
Patients who received the specific left hip fracture nail model (125mm, 13mm x 360mm) from Zimmer Biomet are affected. Those with this exact model are most at risk due to the potential for improper fixation.
Check for the product name 'Affixus Hip Fracture Nail Left 125mm' with dimensions 13mm x 360mm and item number 814413360. This model was sold under specific batch codes: 054030, 054040, 312200, 312210.
Verify the product name, dimensions, and item number to confirm if your nail is part of the recall.
This recall applies to specific left hip fracture nails with the model number 125mm, 13mm x 360mm, and item number 814413360. Check your product details to see if you are affected.
The recall does not specify a remedy, so you should check with Zimmer Biomet directly for guidance on next steps.
Look for the product name 'Affixus Hip Fracture Nail Left 125mm', dimensions 13mm x 360mm, and item number 814413360. This model was sold under batch codes 054030, 054040, 312200, or 312210.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-3103-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3103-2018 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.
