Class II โ€” Potential Health Hazard

Potential health hazard โ€” use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Ventolin HFA (albuterol sulfate) Inhalation Aerosol 90 mcg per actuation Recalled by GlaxoSmithKline Inc Due to Does Not Deliver Proper Metered Dose: Potential content...

Date: July 26, 2012
Company: GlaxoSmithKline Inc
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact GlaxoSmithKline Inc directly.

Affected Products

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

Quantity: 1,412,566 inhalers

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About GlaxoSmithKline Inc

GlaxoSmithKline Inc has 2 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report