Biomet recalls 24mm short anchor plugs for joint surgery repairs due to potential metal burrs causing surgery extension. 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 short anchor plugs used in joint surgery repairs because metal burrs in the device may prevent proper surgical tools from passing through, requiring additional surgery. This poses a risk of extended 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 risks of complications and longer recovery periods.
Surgical patients who received the recalled Compress Device Short Anchor Plug 24mm for joint repair procedures. Surgeons and medical teams using the device during revision surgeries are most at risk.
Check for the item number 178566 and lot numbers listed in the recall: 535440, 577570, 577590, 608770, 671520, 671530, 671880, 671880R, 735750, 735750R, and 965240. These are specific to the Compress Device Short Anchor Plug 24mm used in joint surgery revisions.
Look for the lot numbers listed in the recall: 535440, 577570, 577590, 608770, 671520, 671530, 671880, 671880R, 735750, 735750R, and 965240.
The Compress Device Short Anchor Plug 24mm used for correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement.
Check for the item number 178566 and lot numbers listed: 535440, 577570, 577590, 608770, 671520, 671530, 671880, 671880R, 735750, 735750R, and 965240.
The recall does not specify a remedy, so contact Biomet directly for guidance on next steps.
We’ve drafted a message you can send Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-0386-2024 — Biomet Biomet Hello, I own a Biomet that is covered by recall Z-0386-2024 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.
