Pharmakon Pharmaceuticals, Inc. recalls Ketamine 2 mg/mL in 0.9% Sodium Chloride 30 mL fill in a 35 mL Monoject Plungerless syringe, Rx Only, Compounded by PHAR
Recalled July 20, 2016 · FDA recall D-1329-2016 · Pharmakon Pharmaceuticals
Hazard
Lack of Assurance of Sterility · FDA Class II
Units
150
Sold at
Nationwide VA/DOD: CA, KY, MD, NC, OK, TX, VA
Description
Lack of Assurance of Sterility
Product
Ketamine 2 mg/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 45183-0938-68
Manufacturer(s)
Pharmakon Pharmaceuticals, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →