Teleflex Medical recalls LMA(TM) MADgic(TM) Laryngo-Tracheal Mucosal Atomization Devices: (a) MAD600 MADgic, (b) MAD700 MADgic, (c) MAD720 MADg

Recalled October 4, 2017 · FDA recall Z-3212-2017 · Teleflex Medical

Hazard

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

Units

135,456 units

Sold at

Nationwide distribution

Description

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

Product

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

Manufacturer(s)

Teleflex Medical

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →