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Open, Classified

JuggerLoc/ToggleLoc 2.9mm Drill Guide, Model number 110027357

FDA Recall Z-0477-2025 · Posted 2024-11-15

Recalling FirmBiomet, Inc.
Recall StatusOpen, Classified
Product CodeKDD
Date Initiated2024-10-21
Product Quantity691 (US); 2,045 (OUS)

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.

Firm Action

Pending

Root Cause

Process control

Distribution Pattern

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

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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