Pharmakon Pharmaceuticals, Inc. recalls Hydromorphone HCI 0.4mg/mL in 0.9% Sodium Chloride 30 mL fill in a 35 mL Monoject Plungerless syringe, Rx Only, Compound
Recalled July 20, 2016 · FDA recall D-1292-2016 · Pharmakon Pharmaceuticals
Hazard
Lack of Assurance of Sterility · FDA Class II
Units
20
Sold at
Nationwide VA/DOD: CA, KY, MD, NC, OK, TX, VA
Description
Lack of Assurance of Sterility
Product
Hydromorphone HCI 0.4mg/mL in 0.9% Sodium Chloride 30 mL fill in a 35 mL Monoject Plungerless syringe, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0684-68
Manufacturer(s)
Pharmakon Pharmaceuticals, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →