Biomet recalls 14mm 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 14mm 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 to patients undergoing joint repair procedures.
The anchor plugs may contain metal burrs in the transverse holes, which can prevent drill bits or pins from passing through the device. This could force surgeons to extend the surgery to fix the issue, increasing risks for patients.
Patients who have received the recalled 14mm Segmental Anchor Plugs for revision surgeries are most at risk. The device is used in joint repair procedures after failed osteotomy or arthrodesis.
Check if your device has the item number 178404 and lot numbers listed in the recall notice: 017900, 017900R, 240760, 332020, 332040, 608500, 608590, 671670, 712220, 752770, 798020, or 965310.
Verify your device has the item number 178404 and one of the listed lot numbers from the recall notice.
The anchor plugs may have metal burrs in the transverse holes, preventing drill bits or pins from passing through, which could require surgery to be extended.
Check if your device has the item number 178404 and one of the listed lot numbers from the recall notice. If you have the device, contact Biomet for further instructions.
The recall notice does not specify a fix or remedy for the device.
We’ve drafted a message you can send Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-0372-2024 — Biomet Biomet Hello, I own a Biomet that is covered by recall Z-0372-2024 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.
