Home / Recalls / Teleflex Medical Europe Ltd / Z-1628-2018

Z-1628-2018 Class II Terminated

Recalled by Teleflex Medical Europe Ltd — Athlone, N/A

Recall Details

Product Type
Devices
Report Date
May 9, 2018
Initiation Date
March 19, 2018
Termination Date
August 27, 2019
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
25 units

Product Description

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

Reason for Recall

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

Distribution Pattern

TX

Code Information

Lot Number 161212

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