AstraZeneca recalls Airsupra inhalers with defective delivery systems. These albuterol/budesonide inhalers may not deliver medication properly. Stop using and contact for details.
Defective delivery system
AstraZeneca is recalling Airsupra inhalers that have a defective delivery system. This could mean the medication isn't delivered properly to your lungs. If you have these inhalers, stop using them and contact AstraZeneca for instructions.
The inhaler's delivery system is defective, which may cause the medication to not reach your lungs effectively. This could lead to improper treatment of respiratory conditions like asthma. However, the recall does not specify a risk of serious injury or death.
People who have the Airsupra inhalers with the specific lot numbers and expiration dates listed in the recall. Those with asthma or respiratory conditions are most at risk.
Check the product label for the lot numbers and expiration dates listed: 120-inhalation canisters with lots 6270044C00, 6270040D00, etc., expiring through 10/2026 to 9/30/2027, or 28-inhalation canisters with lots 6270019E00, expiring 7/31/2025.
Immediately stop using the recalled Airsupra inhalers with the specific lot numbers and expiration dates listed in the recall.
The inhaler has a defective delivery system that may not deliver medication properly to your lungs.
Stop using it immediately and contact AstraZeneca for instructions on how to return it.
The recall does not specify a risk of serious injury or death; the hazard is a potential failure to deliver medication effectively.
We’ve drafted a message you can send AstraZeneca to request your refund or repair — edit it as you like.
Subject: Recall D-0444-2025 — AstraZeneca AstraZeneca Hello, I own a AstraZeneca that is covered by recall D-0444-2025 from AstraZeneca. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
