FDAMarch 19, 2018device
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
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Teleflex Medical is recalling the affected product because there may be missing or incomplete information on the package label.
What to do
FDA enforcement status: Terminated
Brands named
teleflex medical europeteleflexteleflex medical
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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- FDALidocaine HCl Injection USP, 25x5 mL, Single-Dose Ampules, Rx Only, Distributed by: Spectra Medical Devices, LLC, Wilmington, Made in S. Korea, NDC 65282-1605-1.2026-05-12
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