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
Reported: May 9, 2018 Initiated: March 19, 2018 #Z-1628-2018
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.
Details
- Recalling Firm
- Teleflex Medical Europe Ltd
- Units Affected
- 25 units
- Distribution
- TX
- Location
- Athlone, N/A
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Teleflex Medical Europe Ltd. Units affected: 25 units.
Why was this product recalled? ▼
Teleflex Medical is recalling the affected product because there may be missing or incomplete information on the package label.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on May 9, 2018. Severity: Moderate. Recall number: Z-1628-2018.
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