Pharmakon Pharmaceuticals, Inc. recalls Ketamine 50mg/mL in 0.9% Sodium Chloride 1mL fill in 3 mL syringe, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Nob
Recalled July 20, 2016 · FDA recall D-1287-2016 · Pharmakon Pharmaceuticals
Hazard
Lack of Assurance of Sterility · FDA Class II
Units
200
Sold at
Nationwide VA/DOD: CA, KY, MD, NC, OK, TX, VA
Description
Lack of Assurance of Sterility
Product
Ketamine 50mg/mL in 0.9% Sodium Chloride 1mL fill in 3 mL syringe, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC # 45183-0603-78
Manufacturer(s)
Pharmakon Pharmaceuticals, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →