La Habra, CA, United States
Auro Pharmacies Inc. DBA Central Drugs recalls
1 recall recorded since 2018, most recently on 22 March 2019. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)0
Terminated Class III Drugs
- Recall started
- 22 March 2019
- Terminated
- 27 February 2020
- Reason
- Failed pH Specification: product does not meet pH label claim.
- Distribution
- Nationwide within the United States
- Initiated
- Voluntary: Firm initiated
- Recall number
- D-1082-2019
- Biotin 10 mg/mL Injection, 30 mL vial, Rx only, 511 S. Harbor Blvd., Building. F, La Habra, CA 90631, 562-352-9630.
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.