FDAClass IIOctober 4, 2017

LMA(TM) MADgic(TM) Laryngo-Tracheal Mucosal Atomization recall

LMA(TM) MADgic(TM) Laryngo-Tracheal Mucosal Atomization Devices: (a) MAD600 MADgic, (b) MAD700 MADgic, (c) MAD720 MADgic Intended for the application…

Why was LMA(TM) MADgic(TM) Laryngo-Tracheal Mucosal Atomization recalled?

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

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot Numbers: (a) MAD600 MADgic: 161217, 161218, 161228 (b) MAD700 MADgic: 161119, 161120, 161121, 161153, 161173, 161212, 161223, 161236 (c) MAD720 MADgic: 161154

Product
LMA(TM) MADgic(TM) Laryngo-Tracheal Mucosal Atomization Devices: (a) MAD600 MADgic, (b) MAD700 MADgic, (c) MAD720 MADgic Intended for the application…
Recalling firm
Teleflex Medical
Quantity
135,456 units
Distribution
Nationwide distribution
Recall date
October 4, 2017
Classification
Class II
Status
Terminated
Agency
FDA (device)
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