Biotin 10 mg/mL Injection — Class III drug recall D-1082-2019
Terminated recall by Auro Pharmacies Inc. DBA Central Drugs, reported 2019-04-17, distributed nationwide. Failed pH Specification: product does not meet pH label claim.
| Recall number | D-1082-2019 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Auro Pharmacies Inc. DBA Central Drugs, La Habra, CA, United States |
| Recall initiated | 2019-03-22 |
| Classified | 2019-04-05 |
| Reported by FDA | 2019-04-17 |
| Terminated | 2020-02-27 |
| Distributed | Nationwide (US) |
| Quantity | 167 vials |
| Reason classes | labeling |
| Expiration dates | 2019-08-04 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1082-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.