FDA recall Z-3212-2017

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

Reason for recall

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

Distribution

Nationwide distribution

Key facts

Status

Terminated

Initiation date

2017-07-05

Report date

2017-10-04

Termination date

2018-11-20

Voluntary/Mandated

Voluntary: Firm initiated

Location

Research Triangle Park, NC, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3212-2017