Medaus, Inc. recalls NANDROLONE DEC 200MG/ML W/PRES. (BENZYL ETOH 10%), In a) 2ML Vials, b) 4ML Vials, and c) 5ML Vials, MEDAUS PHARMACY
Recalled July 20, 2016 · FDA recall D-1230-2016 · Medaus
Hazard
Lack of Assurance of Sterility · FDA Class II
Units
400 mL in Vials
Sold at
U.S. Nationwide, Japan, and New Zealand.
Description
Lack of Assurance of Sterility
Product
NANDROLONE DEC 200MG/ML W/PRES. (BENZYL ETOH 10%), In a) 2ML Vials, b) 4ML Vials, and c) 5ML Vials, MEDAUS PHARMACY
Manufacturer(s)
Medaus, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →