Biomet recalls short anchor plugs for joint surgery repairs due to potential metal burrs causing surgery to extend. Affected items have specific lot numbers and sizes.
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 short anchor plugs used in joint surgery repairs because metal burrs in the device may prevent proper drilling, requiring surgery to be extended. This poses a risk of longer procedures and complications for patients.
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 like longer operative time and potential complications.
Patients who have received the recalled short anchor plugs for joint surgery repairs are most at risk. Surgeons using these specific models during procedures may also be affected.
Check for the product name 'Compress Device Short Anchor Plug, 18 MM' with specific lot numbers listed in the recall notice. The affected items include models with lot numbers starting with 331780, 331790, 331810, 507020, 507020R, 608550, 608700, 671490, or 671850 and 857020.
Identify the lot number on the device or packaging to confirm if it's affected.
Reach out to Biomet directly for further guidance on the recall.
The anchor plugs may have metal burrs that prevent the drill from passing through, potentially extending surgery time.
Check the lot number against the list provided in the recall notice and contact Biomet for further instructions.
Yes, metal burrs could cause surgery to extend, increasing risks like longer procedures and complications.
We’ve drafted a message you can send Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-0382-2024 — Biomet Biomet Hello, I own a Biomet that is covered by recall Z-0382-2024 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.
