RECALL ALERT: Venolin HFA Inhaler – If You or Someone You Know Uses This PLEASE Share


We had an orignal recall back in 2017 of these inhalers. You can see that Post here —>> RECALL ALERT – Do You or Someone You Know Use Ventolin? Then You MUST Read This

There was actually an update that was done, but just now seems to be making its rounds. Due to so many people using these I thought I would still get the information out there since some have no expired yet.


GlaxoSmithKline is voluntarily recalling 593,088 Ventolin HFA 200D albuterol inhalers because of a potentially defective delivery system, according to an FDA enforcement report. The three affected lot numbers are 6ZP9848 (expiration date 3/18), 6ZP0003 (expiration date 4/18), and 6ZP9944 (expiration date 4/18). The devices have been recalled from hospitals, pharmacies, retailers, and wholesalers in the United States.

“There is possible risk that the affected inhalers could potentially not deliver the stated number of actuations,” spokesman Juan Carlos Molina wrote in an email. “We continue to investigate the issue in order to identify the root cause and implement appropriate corrective and preventative actions.”

Though the recall is not at the patient level, patients whose inhalers are among the affected lots can contact GlaxoSmithKline’s customer service center at 888-825-5249 with questions. The recall should not affect pharmacy supplies.

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