Mckesson Medical-Surgical Inc. Corporate Office recalls Miralax (Polyethylene Glycol 3350), Powder for Solution, Osmotic Laxative, 30 Once-Daily Doses, Net WT 17.9 OZ (510 g) b
Recalled August 17, 2022 · FDA recall D-1319-2022 · Mckesson Medical-Surgical Inc. Corporate Office
Hazard
CGMP Deviations: products were stored outside the drug label specifications. · FDA Class II
Units
67 bottles
Sold at
Nationwide in the USA.
Description
CGMP Deviations: products were stored outside the drug label specifications.
Product
Miralax (Polyethylene Glycol 3350), Powder for Solution, Osmotic Laxative, 30 Once-Daily Doses, Net WT 17.9 OZ (510 g) bottle, Bayer Healthcare Pharmaceuticals, NDC 11523-7234-4.
Manufacturer(s)
Mckesson Medical-Surgical Inc. Corporate Office
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →