Biomet recalls short anchor plugs (16mm) for joint repair surgeries due to potential metal burrs causing surgery to extend. Affected items have specific lot numbers and item numbers. Consumers should contact Biomet for details.
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 repair surgeries 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 the risk of complications and longer recovery periods.
Patients who have undergone joint replacement surgery or revision procedures using the recalled anchor plugs are most at risk. Surgeons and medical facilities that used these specific models during procedures may also be affected.
Check if your device has the item number 178558 and lot numbers listed in the recall notice (e.g., 331750, 331760, 331770, etc.). The product is used for correcting revision of unsuccessful osteotomy, arthrodesis, or previous joint replacements.
Reach out to Biomet directly to confirm if your specific device is affected and get instructions for replacement or correction.
The anchor plugs may have metal burrs that prevent the drill or pins from passing through, potentially extending surgery time.
Check for the item number 178558 and lot numbers listed in the recall notice (e.g., 331750, 331760, 331770, etc.).
Contact Biomet directly to confirm if your device is affected and get instructions for replacement or correction.
We’ve drafted a message you can send Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-0381-2024 — Biomet Biomet Hello, I own a Biomet that is covered by recall Z-0381-2024 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.
