FDA recall D-1082-2019
Auro Pharmacies Inc. DBA Central Drugs · Class III · drug
Product
Biotin 10 mg/mL Injection, 30 mL vial, Rx only, 511 S. Harbor Blvd., Building. F, La Habra, CA 90631, 562-352-9630.
Reason for recall
Failed pH Specification: product does not meet pH label claim.
Distribution
Nationwide within the United States
Key facts
- Status
- Terminated
- Initiation date
- 2019-03-22
- Report date
- 2019-04-17
- Termination date
- 2020-02-27
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- La Habra, CA, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1082-2019