US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jul 26, 2012 (14 years ago)

Ventolin HFA (albuterol sulfate) Inhalation Aerosol 90 mcg per actuation, 200 Metered…

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

Why it was recalled

Does Not Deliver Proper Metered Dose: Potential content of albuterol per dose is below specification.

What was recalled

Ventolin HFA (albuterol sulfate) Inhalation Aerosol 90 mcg per actuation, 200 Metered Inhalations, FOR ORAL INHALATION ONLY - For use with Ventolin HFA actuator only. Net. wt. 18 g Rx only, GlaxoSmithKline, Reasearch Triangle Park, NC 27709 NDC 0173-0682-20

Recalling firm
GlaxoSmithKline Inc
NDC code
0173-0682-20
Origin
NC, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1666-2012

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.

Other Albuterol recalls

See all