Class II

Medical Device Recall: JuggerLoc/ToggleLoc 2.9mm Drill Guide, Model number 110027357

Biomet, Inc. · October 21, 2024

Reason for Recall

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.

Distribution

Worldwide distribution - US Nationwide and the countries of Australia, Brazil, Canada, Singapore, Switzerland.

States Affected

NATIONWIDE

Quantity Affected

691 (US); 2,045 (OUS)

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0477-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.