US Drug Recall Register
Class III · Low risk Terminated Initiated Dec 12, 2023 (3 years ago)

ANORO ELLIPTA (umeclidinium and vilanterol inhalation powder) 62.5 mcg/25mcg. 1 inhaler…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Failed Release Testing: Coarse Particle Mass for umeclidinium Out of Specification

What was recalled

ANORO ELLIPTA (umeclidinium and vilanterol inhalation powder) 62.5 mcg/25mcg. 1 inhaler contains 30 doses (60 blisters total), Rx Only, Manufactured by GlaxoSmithKline Durham, NC 27701. NDC 0173-0869-10

Recalling firm
GlaxoSmithKline LLC
NDC code
0173-0869-10
Origin
NC, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0160-2024

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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