Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Ventolin HFA (albuterol sulfate) Inhalation Recalled by GlaxoSmithKline, LLC Due to Defective Delivery System: Elevated number of units with...
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, 90 mcg per actuation, 200 Metered Inhalations, Net Wt. 18 g inhalers, Rx only, GlaxoSmithKline, Research Triangle Park, NC 27709, NDC 0173-0682-20.
Quantity: 562,883
Why Was This Recalled?
Defective Delivery System: Elevated number of units with out of specification results for leak rate
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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