Drug Recall: 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, M
AsttraZeneca Pharmaceuticals LP · May 14, 2025
Reason for Recall
Defective delivery system
Product Description
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, .
Distribution
USA Nationwide
States Affected
NATIONWIDE
Quantity Affected
a) 807,837 canisters; b) 235,698 canisters
Source: FDA (openFDA Drug Enforcement)
Recall number: D-0444-2025
Status: ongoing
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