Drug recall
Biotin 10 mg/mL Injection, 30 mL vial, Rx only, 511 S. Harbor Blvd., Building. F, La Habra, CA 90631…
FDA recall event 82483 · Class III · Auro Pharmacies Inc. DBA Central Drugs
Key facts
| Event ID | 82483 |
|---|---|
| Recall numbers | D-1082-2019 |
| Recalling firm | Auro Pharmacies Inc. DBA Central Drugs |
| Product type | Drugs |
| Products | Biotin 10 mg/mL Injection, 30 mL vial, Rx only, 511 S. Harbor Blvd., Building. F, La Habra, CA 90631, 562-352-9630. |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Failed pH Specification: product does not meet pH label claim. |
| Initiation date | Mar 22, 2019 |
| Report date | Apr 17, 2019 |
| Termination date | Feb 27, 2020 |
| City | La Habra |
| State | CA |
| Country | United States |
| FEI number | 3012228279 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: