FDA recall D-1640-2019
RXQ Compounding LLC · Class II · drug
Product
BUFFERED LIDOCAINE HCL 1% INJECTION SOL (PF) SYR, 0.5 ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0139-84
Reason for recall
Lack of Assurance of Sterility
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-1640-2019