Biomet recalls 24mm Segmental Anchor Plugs for revision surgeries due to potential metal burrs causing surgery to extend. Affected items have 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 24mm Segmental Anchor Plugs used in revision surgeries because metal burrs in the device may prevent proper drilling, requiring surgery to be extended. This risk affects patients who have recently had joint surgery.
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 risks for patients.
Patients who have received the recalled 24mm Segmental Anchor Plugs for revision surgeries after unsuccessful osteotomy or joint replacement are most at risk. The device is used in specific orthopedic procedures.
Check for the item number 178414 and specific lot numbers including 017930, 018070, 608560, 752820, and 752830. The product is sold for revision of joint surgery procedures.
Review the item number 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.
The recall notice does not specify a remedy, so check the product details to see if it is affected.
Look for item number 178414 and specific lot numbers including 017930, 018070, 608560, 752820, or 752830.
We’ve drafted a message you can send Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-0377-2024 — Biomet Biomet Hello, I own a Biomet that is covered by recall Z-0377-2024 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.
