Teleflex Medical Lma(tm) Madgic(tm) Laryngo-tracheal recall
Teleflex MEDICAL LMA(TM) MADgic(TM) LARYNGO-TRACHEAL MUCOSAL ATOMIZATION DEVICE, MAD700, QTY: 1 Intended for the application of topical anesthetics to…
Why was Teleflex Medical Lma(tm) Madgic(tm) Laryngo-tracheal 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 Number 161212
- Product
- Teleflex MEDICAL LMA(TM) MADgic(TM) LARYNGO-TRACHEAL MUCOSAL ATOMIZATION DEVICE, MAD700, QTY: 1 Intended for the application of topical anesthetics to…
- Recalling firm
- Teleflex Medical Europe Ltd
- Quantity
- 25 units
- Distribution
- TX
- Recall date
- May 9, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)