FDA recall D-1635-2019

RXQ Compounding LLC · Class II · drug

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

Reason for recall

Crystallization

Distribution

Nationwide USA

Key facts

Status
Terminated
Initiation date
2019-06-19
Report date
2019-08-14
Termination date
2022-09-16
Voluntary/Mandated
Voluntary: Firm initiated
Location
Athens, OH, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1635-2019