Biomet recalls 12mm Segmental Anchor Plugs for revision surgeries due to potential metal burrs causing extended procedures. 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 12mm Segmental Anchor Plugs used in joint surgery revisions because metal burrs in the device may prevent proper drilling, requiring additional surgery. This affects patients who had recent joint surgery revisions.
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 received the recalled 12mm Segmental Anchor Plugs for revision surgeries after unsuccessful osteotomy, arthrodesis, or joint replacement. Those with the specific lot numbers listed in the recall are most at risk.
Check if your device has the item number 178402 and lot numbers from the list provided in the recall (e.g., 240750, 671330, 921660, etc.). The product is used for revision surgeries after joint replacements.
Identify if your device has the item number 178402 and the specific lot numbers listed in the recall.
The anchor plugs may contain metal burrs that prevent proper drilling, potentially requiring additional surgery.
Check if your device has the item number 178402 and the specific lot numbers listed in the recall. If you have the recalled item, contact Biomet for further instructions.
Look for the item number 178402 and lot numbers from the list provided in the recall (e.g., 240750, 671330, 921660, etc.).
We’ve drafted a message you can send Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-0371-2024 — Biomet Biomet Hello, I own a Biomet that is covered by recall Z-0371-2024 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.
