FDAFDA · Food and drugs·Recall number Z-1628-2018
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
Published May 9, 2018 · Recall initiated: March 19, 2018
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Teleflex Medical is recalling the affected product because there may be missing or incomplete information on the package label.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Teleflex Medical Europe Ltd
- Distributor
- TX
- Lot
- Lot Number 161212
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- Ireland
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