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VENTOLIN DISKUS devices carrying the recalled lot number 786G should be returned to your local pharmacy for replacement. VENTOLIN metered dose inhalers, commonly referred to as “puffers” (tradename “VENTOLIN HFA”) are not affected by this issue and patients can continue to use as prescribed by their healthcare professional. We have carried out a thorough investigation and the root cause of the issue has been corrected. We are committed to supplying high-quality products to Canadian patients and sincerely regret any inconvenience patients and healthcare professionals may experience related to this recall. GSK enquiries: Corporate Communications +1 905-819-3363 (Mississauga) +1 450-680-4812 (Laval) Read more↗

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Keywordsglaxosmithkline notification recall ventolin diskus lot 786g 16feb2018 pdf feb
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