US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Mar 22, 2017 (9 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

Defective Delivery System: Elevated number of units with out of specification results for leak rate.

What was recalled

Ventolin HFA (albuterol sulfate) Inhalation Aerosol, 90 mcg per actuation, 200 Metered Inhalations, Net Wt. 18 g inhalers, Rx only, GlaxoSmithKline, Research Triangle Park, NC 22709, NDC 0173-0682-20.

Recalling firm
GlaxoSmithKline, LLC
NDC code
0173-0682-20
Origin
NC, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0626-2017

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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