SCA Pharmaceuticals, LLC recalls Ketamine 50 mg/5 mL in 0.9% Sodium Chloride Injection for IV or IM Use (concentration = 10 mg/mL), 6 mL Syringe, Rx Only
Recalled August 28, 2019 · FDA recall D-1843-2019 · SCA Pharmaceuticals
Hazard
Lack of Assurance of Sterility. · FDA Class II
Units
922 syringes
Sold at
Nationwide in the U.S.
Description
Lack of Assurance of Sterility.
Product
Ketamine 50 mg/5 mL in 0.9% Sodium Chloride Injection for IV or IM Use (concentration = 10 mg/mL), 6 mL Syringe, Rx Only, SCA Pharmaceuticals, Windsor, CT 06095, NDC 70004-0430-09.
Manufacturer(s)
SCA Pharmaceuticals, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →