Biomet recalls 10mm Segmental Anchor Plugs for revision surgeries due to potential metal burrs causing surgery to extend. Affected items have specific lot numbers and item numbers.
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 10mm Segmental Anchor Plugs used in revision surgeries because metal burrs in the device may prevent proper drilling, requiring surgery to be extended. This poses a risk of longer procedures and complications.
The anchor plugs may contain metal burrs that block the drill or pins from passing through the device. This can cause the surgery to extend beyond the intended time, increasing the risk of complications and longer recovery periods.
Surgical patients who have received the recalled 10mm Segmental Anchor Plugs for revision surgeries are affected. Surgeons and medical staff using the device during procedures are at higher risk.
Check the item number on the device, which is 178400. Look for specific lot numbers: 541470, 608490, 608580, 609140, 671410, 671650, or 856920.
Verify the item number (178400) and lot numbers listed in the recall notice to confirm if your device is affected.
The anchor plugs may have metal burrs that prevent the drill or pins from passing through, causing surgery to extend.
Check the item number (178400) and lot numbers to confirm if your device is affected. The recall does not specify a remedy, so contact Biomet directly for guidance.
Yes, affected lot numbers include 541470, 608490, 608580, 609140, 671410, 671650, and 856920.
We’ve drafted a message you can send Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-0370-2024 — Biomet Biomet Hello, I own a Biomet that is covered by recall Z-0370-2024 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.
