Biomet recalls 2.9mm Drill Guides (Model 110027357) due to warping in packaging that may delay surgery or cause tissue reactions. Affected units include specific lots sold in the US.
Firm received complaints reporting that guides were warped when pulled out of packaging. This issue may result in extension of surgery to find another product, or may lead to adverse local tissue reaction leading to surgical intervention.
Biomet is recalling its 2.9mm Drill Guides (Model 110027357) because they can warp when taken out of packaging. This might cause surgery to be delayed or lead to tissue reactions requiring additional medical intervention.
The guides can warp when removed from packaging, which might cause surgery to be delayed or lead to tissue reactions that require additional medical procedures.
Surgical patients using the recalled drill guides are most at risk. The recall affects specific lots of the 2.9mm Drill Guides sold in the US.
Check for the model number 110027357 on the product. Affected units include specific lots listed in the recall notice (e.g., 0002446326 through 0002614123).
Look for the lot numbers listed in the recall notice (e.g., 0002446326 through 0002614123) on the product packaging.
Biomet received complaints that the guides warp when pulled out of packaging, which may delay surgery or cause tissue reactions requiring additional medical intervention.
Check the product for the lot numbers listed in the recall notice (e.g., 0002446326 through 0002614123). If you have the affected lot, contact Biomet for further instructions.
The recall does not mention a fix or remedy. Affected units should be checked against the listed lot numbers.
We’ve drafted a message you can send Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-0477-2025 — Biomet Biomet Hello, I own a Biomet that is covered by recall Z-0477-2025 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.
