US Drug Recall Register
Class II · Moderate risk Terminated Initiated Mar 26, 2024 (2 years ago)

Ipratropium Bromide and Albuterol Sulfate Inhalation Solution USP, 0.5 mg & 3mg/3mL…

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

Why it was recalled

Short fill: Complaints received of less fill volume in respule and few drops of liquid observed in the intact pouch.

What was recalled

Ipratropium Bromide and Albuterol Sulfate Inhalation Solution USP, 0.5 mg & 3mg/3mL unit-dose vials, packaged in carton containing 30 vials ( 6 pouches of 5 - 3 mL vials), Rx only, Manufactured by: Cipla Ltd., Indore SEZ, Pithampur, India, Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059, NDC 69097-173-53

Recalling firm
Cipla USA, Inc.
NDC code
69097-173-53
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0471-2024

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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