Pharmakon Pharmaceuticals, Inc. recalls Hydromorphone HCI 1 mg/mL in 0.9% Sodium Chloride, 50 mL lntravia bag IV USE ONLY, Rx Only, Compounded by PHARMAKON Pha
Recalled July 20, 2016 · FDA recall D-1312-2016 · Pharmakon Pharmaceuticals
Hazard
Lack of Assurance of Sterility · FDA Class II
Units
675
Sold at
Nationwide VA/DOD: CA, KY, MD, NC, OK, TX, VA
Description
Lack of Assurance of Sterility
Product
Hydromorphone HCI 1 mg/mL in 0.9% Sodium Chloride, 50 mL lntravia bag IV USE ONLY, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060 , NDC 45183-0865-41
Manufacturer(s)
Pharmakon Pharmaceuticals, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →