US Drug Recall Register
Class I · High risk Terminated Initiated Jun 27, 2023 (3 years ago)

Albuterol Sulfate Inhalation Aerosol, 90 mcg, 200 Metered Inhalation, net content 6.7 g…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Defective container: empty inhaler and leakage observed through the inhaler valve due to partially missing bottom seat (gasket).

What was recalled

Albuterol Sulfate Inhalation Aerosol, 90 mcg, 200 Metered Inhalation, net content 6.7 g canister packaged in a box, Rx only, Manufactured by: Cipla Ltd, Indore SE Z, Pithampur, India, Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ, 07059, NDC 69097-142-60

Recalling firm
Cipla USA, Inc.
NDC code
69097-142-60
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0938-2023

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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