US Drug Recall Register
Class II · Moderate risk Ongoing Initiated May 14, 2025 (16 months ago)

Airsupra (albuterol and budesonide) inhalation aerosol, 90 mcg/80 mcg per inhalation…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Defective delivery system

What was recalled

Airsupra (albuterol and budesonide) inhalation aerosol, 90 mcg/80 mcg per inhalation, packaged in a) 120-inhalation canister (NDC 0310-9080-12) b) 28-inhalation canister (NDC 0310-9080-28), Rx only, Manufactured for: AstraZeneca Pharmaceuticals LP, Wilmington, DE 19850, By: AstraZeneca Dunkerque Production (AZDP), Dunkerque, France, Product of France, .

Recalling firm
AsttraZeneca Pharmaceuticals LP
NDC code
0310-9080-12
Origin
DE, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0444-2025

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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