Biomet, Inc. recalls JuggerLoc/ToggleLoc 2.9mm Drill Guide, Model number 110027357

Recall date

October 21, 2024

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-0477-2025

FDA classification

Class II

Brand / firm

Biomet, Inc.

Sold / distributed

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

Why it was 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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

JuggerLoc/ToggleLoc 2.9mm Drill Guide, Model number 110027357