Teleflex Medical Europe Ltd recalls Teleflex MEDICAL LMA(TM) MADgic(TM) LARYNGO-TRACHEAL MUCOSAL ATOMIZATION DEVICE, MAD700, QTY: 1 Intended for the applic…

Recall date

March 19, 2018

Source

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

Recall number

Z-1628-2018

FDA classification

Class II

Brand / firm

Teleflex Medical Europe Ltd

Sold / distributed

TX

Why it was recalled

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

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

What was recalled

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