FDAJuly 5, 2017device

LMA(TM) MADgic(TM) Laryngo-Tracheal Mucosal Atomization Devices: (a) MAD600 MADgic, (b) MAD700 MADgic, (c) MAD720 MADgic Intended for the application of topical anesthetics to the oropharynx and upper airway region

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

The hazard

Teleflex Medical is recalling the affected product because there may be missing or incomplete information on the package label.

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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