Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
JuggerLoc/ToggleLoc 2.9mm Drill Guide Recalled by Biomet, Inc. Due to Firm received complaints reporting that guides were warped...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Biomet, Inc. directly.
Affected Products
JuggerLoc/ToggleLoc 2.9mm Drill Guide, Model number 110027357
Quantity: 691 (US); 2,045 (OUS)
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Biomet, Inc.
Biomet, Inc. has 250 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report