Biomet recalls 18mm Segmental Anchor Plugs with potential metal burrs that could prevent drill passage, requiring surgery extension. Affected items include specific lot numbers and item codes.
Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
Biomet is recalling 18mm Segmental Anchor Plugs used in joint surgery repairs because metal burrs in the device might prevent drill pins from passing through, potentially requiring surgery to be extended. This recall affects specific lot numbers and item codes.
The anchor plugs may contain metal burrs in the transverse holes, which can block drill pins from passing through. This could force surgeons to extend the surgery to fix the issue, increasing risks during the procedure.
Orthopedic surgeons and medical professionals who use Biomet's Segmental Anchor Plugs for joint repairs are most at risk. Patients who have received these implants may also be affected.
Check for the product name 'Compress Device Segmental Anchor Plug, 18 MM' with specific lot numbers: 017910, 017910R, 018060, 332060, 608610, 671740, 671740R, 752790, 752790R, and 965290.
Identify the lot numbers and item codes listed in the recall notice to confirm if your device is affected.
The anchor plugs may have metal burrs in the transverse holes that prevent drill pins from passing through, potentially requiring surgery extension.
Check the product details against the listed lot numbers and item codes to see if it's affected. If it is, contact Biomet for further instructions.
The recall is for medical professionals using the device during surgery. Patients who have received the implant may need to consult their surgeon about potential risks.
We’ve drafted a message you can send Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-0374-2024 — Biomet Biomet Hello, I own a Biomet that is covered by recall Z-0374-2024 from 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.
