Zimmer Biomet recalls specific hip fracture nail models due to set screw malfunction. Affected items may not advance or reverse properly, potentially causing improper fixation. Contact for return instructions.
The set screw is not able to advance or reverse from the original position in the nail.
Zimmer Biomet is recalling certain hip fracture nail models because the set screw can't move correctly. This could lead to improper bone fixation and complications after surgery.
The set screw in the nail fails to advance or reverse from its original position. This could cause improper bone fixation during surgery, potentially leading to complications after the procedure.
Surgical patients who received the recalled hip fracture nail models during procedures. Patients with the specific item numbers are most at risk.
Check for the item numbers 814613360 or 816070 091850 on the nail packaging or product label. The product is a left hip fracture nail with a 13 mm x 360 mm size.
Verify the item number on the nail packaging or label to confirm if it's affected.
The set screw cannot advance or reverse from its original position, which may cause improper bone fixation during surgery.
Check for item numbers 814613360 or 816070 091850 on the nail packaging or label.
The recall record does not specify a remedy, so contact Zimmer Biomet directly for instructions.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-3168-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3168-2018 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.
