RXQ Compounding LLC recalls Ascorbic Acid 400 MG/ML (Non-Corn) Injection Solution, 65 mL per vial, RXQ Compounding, 340 West State Street, Unit 9, A
Recalled August 14, 2019 · FDA recall D-1635-2019 · RXQ Compounding
Hazard
Crystallization · FDA Class II
Units
N/A
Sold at
Nationwide USA
Description
Crystallization
Product
Ascorbic Acid 400 MG/ML (Non-Corn) Injection Solution, 65 mL per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0914-65
Manufacturer(s)
RXQ Compounding LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →