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.
- Recall date
- March 22, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-1082-2019
- FDA classification
- Class III
- Brand / firm
- Auro Pharmacies Inc. DBA Central Drugs
- Sold / distributed
- Nationwide within the United States
Why it was recalled
Failed pH Specification: product does not meet pH label claim.
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
Biotin 10 mg/mL Injection, 30 mL vial, Rx only, 511 S. Harbor Blvd., Building. F, La Habra, CA 90631, 562-352-9630.
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