GlaxoSmithKline (GSK) issued a voluntary Class II recall on April 4, 2017 for three lots of Ventolin® HFA 200D Inhalers from U.S. hospitals, pharmacies, retailers and wholesalers as a precautionary measure. It is not a consumer recall.
The lot numbers are:
6ZP0003
6ZP9944
6ZP9848
DH's says Ventolin HFA 90MCG/ACT 200 dose
So that's different right? I don't have his in front of my--just the receipt from the file cabinet. So I do'nt have the lot number.