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Biomet, Inc. recalls JuggerLoc/ToggleLoc 2.9mm Drill Guide, Model number 110027357
Recalled November 27, 2024 · FDA recall Z-0477-2025 · Biomet
Hazard
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. · FDA Class II
Units
691 (US); 2,045 (OUS)
Sold at
Worldwide distribution - US Nationwide and the countries of Australia, Brazil, Canada, Singapore, Switzerland.
Description
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.
Product
JuggerLoc/ToggleLoc 2.9mm Drill Guide, Model number 110027357
Manufacturer(s)
Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →