GSK Plc is voluntarily recalling more than 593,000 Ventolin asthma inhalers from.S. Hospitals, pharmacies, retailers and free ventolin wholesalers due to a defect that may cause them to deliver fewer doses of the ventolin recall medicine than indicated, the British drugmaker said on Tuesday. The company said it had received an elevated number of product complaints about a bulging of the outside wrapper, indicating a leak of the propellant that delivers the medicine. The recall involves three lots of the Ventolin HFA 200D inhalers manufactured at GSKs plant in Zebulon, North Carolina. Food and Drug Administration has approved the voluntary Level 2 recall, which only affects products in the United States, GSK spokesman Juan Carlos Molina said. The defect does not pose a danger to patients, so they are not being asked to return inhalers they have already purchased. GSK said it was trying to identify the root cause of the problem and would take corrective action. Meanwhile, the Zebulon plant is still making the inhalers, Molina said. We currently dont anticipate a supply impact to Ventolin HFA 200D inhaler as a result of this issue, GSK said in a statement. (Reporting by Bill Berkrot; Editing by Lisa Von Ahn). Image via Shutterstock, on April 4, pharmaceutical company GlaxoSmithKline initiated a voluntary recall of 593,000 prescription-only inhalers due to a possible ventolin medication defect. The affected units are being recalled from hospitals, pharmacies, retailers and wholesalers in the United States. According to the, asthma and Allergy Foundation of America, the medication being recalled is Ventolin HFA 200D inhalers. The recall will cover these lots and please note, this is not a consumer-level recall, but its still important to check if your inhaler is affected. The potential defect involves the inhalers delivery system. A GSK representative told the aafa the recall is precautionary and due to complaints about the overwrap (the pouch that holds the inhaler) becoming inflated by leaking from the product. The risk is that the leaking could cause the inhaler to deliver fewer doses than shown on the inhalers counter, leading the user to believe theres more medication in it than there actually. Users of the product are being told not to return it and to call GlaxoSmithKlines response center at if they have questions about their ventolin side effects inhalers efficacy. Advertisement, a statement from GSK to the aafa reads, Though the overall benefit-risk assessment for Ventolin HFA 200D Inhaler when used at prescribed doses remains favourable, in this situation, there is possible risk to patients of experiencing diminished bronchodilation in the setting of acute bronchospasm if reliant. GSK is committed to supplying high quality product and patient satisfaction, and we sincerely regret any inconvenience this recall may cause. Too long, didnt read? The medication itself is still safe to use, the risk is in the patient thinking they have a certain amount of medication left when they might not due to the potential leakage. The aafa says the recall shouldnt affect a pharmacys supplies of the medication if you need a refill of a Ventolin HFA 200D inhaler. GlaxoSmithKline (GSK) has voluntarily recalled 593,088 ventolin recall Ventolin HFA (albuterol sulfate) inhalers due to an issue with the delivery system. Image/The Global Dispatch, according ventolin cost to the US Food and Drug Administration (FDA), there were an elevated number of units with out of specification results for leak rate. The affected lot numbers and expiration dates are Lot 6ZP9848, ventolin recall Exp 03/18; 6ZP0003, 6ZP9944, Exp 04/18. The affected units are being recalled from hospitals, pharmacies, retailers and wholesalers in the United States.. Its not a patient-level recall, but patients whose inhalers are among the affected lots can contact GSKs customer service center at with questions.
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