Auro Pharmacies Inc. DBA Central Drugs recalls Biotin 10 mg/mL Injection, 30 mL vial, Rx only, 511 S. Harbor Blvd., Building. F, La Habra, CA 90631, 562-352-9630.
Recalled April 17, 2019 · FDA recall D-1082-2019 · Auro Pharmacies Inc.
Hazard
Failed pH Specification: product does not meet pH label claim. · FDA Class III
Units
167 vials
Sold at
Nationwide within the United States
Description
Failed pH Specification: product does not meet pH label claim.
Product
Biotin 10 mg/mL Injection, 30 mL vial, Rx only, 511 S. Harbor Blvd., Building. F, La Habra, CA 90631, 562-352-9630.
Manufacturer(s)
Auro Pharmacies Inc. DBA Central Drugs
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →