FDA recall record

ANORO ELLIPTA recall — FDA D-0160-2024

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

Class IIIclassification
D-0160-2024official record ID
Jan 3, 2024report date

Recall record at a glance

Official recordD-0160-2024
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmGlaxoSmithKline LLC
Report dateJan 3, 2024
Recall initiation dateDec 12, 2023
Quantity67,508 inhalers
LocationDurham, NC, United States

Official product description

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

Why the product was recalled

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

Distribution information

Distributed Nationwide in the USA and Puerto Rico.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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