GlaxoSmithKline, a prominent pharmaceutical company, has announced a voluntary recall of approximately 593,000 prescription inhalers due to a potential defect in their delivery system. This recall affects hospitals, pharmacies, retailers, and wholesalers across the United States.
The inhalers in question are the Ventolin HFA 200D. While this recall does not directly target consumers, it is essential for users to verify whether their inhalers are included in the affected lot numbers: 6ZP98486, ZP00036, and ZP9944.
The issue arises from a defect that may cause the inhaler’s pouch to become inflated due to product leakage. A GSK spokesperson clarified to the Asthma and Allergy Foundation of America (AAFA) that this precautionary measure follows reports of the overwrap being compromised, which could lead to the inhaler delivering fewer doses than indicated on its counter. This situation could mislead users into thinking they have more medication available than they actually do.
Users are advised not to return the inhalers but to reach out to GlaxoSmithKline for any questions regarding their inhaler’s performance. GSK expressed that while the overall risk associated with Ventolin HFA 200D remains low, there is a concern that patients relying on a potentially faulty inhaler may experience inadequate bronchodilation during an acute asthma attack.
For those needing a Ventolin HFA 200D inhaler refill, the AAFA assures that this recall should not disrupt pharmacy supplies. It is important to note that the medication itself remains safe for use; the primary concern is the possibility of miscalculating the remaining doses due to leakage.
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In summary, GlaxoSmithKline is recalling nearly 600,000 Ventolin HFA 200D inhalers due to a potential defect in the delivery system that may cause inaccurate dosing. Patients are advised to check their inhalers against the recalled lot numbers and to contact GSK for any concerns.