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Teleflex Medical Europe Ltd recalls Teleflex MEDICAL LMA(TM) MADgic(TM) LARYNGO-TRACHEAL MUCOSAL ATOMIZATION DEVICE, MAD700, QTY: 1 Intended for the applica
Recalled May 9, 2018 · FDA recall Z-1628-2018 · Teleflex Medical Europe
Hazard
Teleflex Medical is recalling the affected product because there may be missing or incomplete information on the package label. · FDA Class II
Units
25 units
Sold at
TX
Description
Teleflex Medical is recalling the affected product because there may be missing or incomplete information on the package label.
Product
Teleflex MEDICAL LMA(TM) MADgic(TM) LARYNGO-TRACHEAL MUCOSAL ATOMIZATION DEVICE, MAD700, QTY: 1 Intended for the application of topical anesthetics to the oropharynx and upper airway region
Manufacturer(s)
Teleflex Medical Europe Ltd
Made in
Ireland
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →