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, .
Reported: May 28, 2025 Initiated: May 14, 2025 #D-0444-2025
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, .
Reason for Recall
Defective delivery system
Details
- Recalling Firm
- AsttraZeneca Pharmaceuticals LP
- Units Affected
- a) 807,837 canisters; b) 235,698 canisters
- Distribution
- USA Nationwide
- Location
- Wilmington, DE
Frequently Asked Questions
What product 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, .. Recalled by AsttraZeneca Pharmaceuticals LP. Units affected: a) 807,837 canisters; b) 235,698 canisters.
Why was this product recalled? ▼
Defective delivery system
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on May 28, 2025. Severity: Moderate. Recall number: D-0444-2025.
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