Pharmakon Pharmaceuticals, Inc. recalls HYDROmorphone HCI 0.2 mg/mL in 0.9% Sodium Chloride 50 mL fill in a 60 mL Monoject Syringe, Rx Only, Compounded by PHARM
Recalled July 20, 2016 · FDA recall D-1326-2016 · Pharmakon Pharmaceuticals
Hazard
Lack of Assurance of Sterility · FDA Class II
Units
120
Sold at
Nationwide VA/DOD: CA, KY, MD, NC, OK, TX, VA
Description
Lack of Assurance of Sterility
Product
HYDROmorphone HCI 0.2 mg/mL in 0.9% Sodium Chloride 50 mL fill in a 60 mL Monoject Syringe, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0933-75
Manufacturer(s)
Pharmakon Pharmaceuticals, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →