Medaus, Inc. recalls MINOXIDIL 0.5% W/PRES. (BENZYL ETOH 2%), 10ML Vials, MEDAUS PHARMACY
Recalled July 20, 2016 · FDA recall D-1226-2016 · Medaus
Hazard
Lack of Assurance of Sterility · FDA Class II
Units
21000 mL in Vials
Sold at
U.S. Nationwide, Japan, and New Zealand.
Description
Lack of Assurance of Sterility
Product
MINOXIDIL 0.5% W/PRES. (BENZYL ETOH 2%), 10ML Vials, MEDAUS PHARMACY
Manufacturer(s)
Medaus, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →