FDAMarch 15, 2021drug

Budesonide and Formoterol Fumarate Dihydrate Inhalation Aerosol 80/4.5 budesonide 80 mcg/formoterol fumarate dihydrate 4.5 mcg Inhalation Aerosol 120 inhalations Rx only Manufactured for: AstraZeneca Pharmaceuticals LP, Wilmington, DE 19850, NDC 0310-7372-20

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

CGMP Deviations: Intermittent exposure to temperature excursion during storage.

What to do

FDA enforcement status: Terminated

Brands named

cardinal healthcardinal

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Budesonide and Formoterol Fumarate Dihydrate Inhalation Aerosol 80/4.5 budesonide 80 mcg/formoterol fumarate dihydrate 4.5 mcg Inhalation Aerosol 120 inhalations Rx only Manufactured for: AstraZeneca Pharmaceuticals LP, Wilmington, DE 19850, NDC 0310-7372-20 — Recall Details · AllClear