FDAJanuary 9, 2020device

Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The products are being recalled due to reports of breakage broke at the point of a welded joint either prior to use during setup or during use inside the patient's mouth.

What to do

FDA enforcement status: Terminated

Brands named

teleflex medicalteleflex

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System — Recall Details · AllClear