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 Recalled by GlaxoSmithKline, LLC Due to Defective Delivery System: Some canisters may not contain...

Date: December 3, 2015
Company: GlaxoSmithKline, LLC
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, LLC directly.

Affected Products

Ventolin HFA (albuterol sulfate) Inhalation Aerosol, 90 mcg per actuation, 200 Metered Inhalations, Rx Only, For Oral Inhalation Only, Net Wt. 18 g, GlaxoSmithKline, Research Triangle Park, NC 27709, NDC 0173-0682-20

Quantity: 128,704 Inhalers

Why Was This Recalled?

Defective Delivery System: Some canisters may not contain sufficient propellant to deliver the labeled claim of 200 actuations through the end of shelf life.

Where Was This Sold?

This product was distributed to 2 states: MS, VT

Affected (2 states)Not affected

About GlaxoSmithKline, LLC

GlaxoSmithKline, LLC has 7 total recalls tracked by RecallDetector.

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