In a significant announcement on April 4, pharmaceutical giant GlaxoSmithKline (GSK) voluntarily recalled approximately 593,000 prescription inhalers due to a potential defect. This recall affects units distributed across hospitals, pharmacies, retailers, and wholesalers throughout the United States.
The inhalers in question are the Ventolin HFA 200D. While this recall is not directed at consumers, it is essential for users to verify if their inhalers are impacted by the recall, which includes the following lot numbers: 6ZP98486, ZP00036, and ZP9944.
The reason for the recall stems from issues with the inhaler’s delivery system. A GSK spokesperson informed the Asthma and Allergy Foundation of America (AAFA) that the recall is precautionary, prompted by reports of the overwrap (the pouch that encloses the inhaler) potentially inflating due to product leakage. This leakage could lead to the inhaler delivering fewer doses than indicated, misleading users about the actual medication remaining.
GSK advises users not to return the inhalers but to contact their response center for any questions regarding the inhaler’s effectiveness. A statement from GSK emphasized, “While the overall benefit-risk assessment for Ventolin® HFA 200D Inhaler remains favorable when used as directed, there is a potential risk of patients experiencing reduced bronchodilation during acute bronchospasm if they depend on a rescue inhaler that may not provide the expected number of doses. GSK is dedicated to delivering high-quality products and ensuring patient satisfaction, and we apologize for any inconvenience caused by this recall.“
To summarize, the medication itself is still safe, but there is a risk of users misjudging the amount of medication left due to potential leakage. The AAFA assures that this recall will not impact pharmacy supplies of the Ventolin HFA 200D inhaler for those needing a refill.
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