# FDA recall D-1082-2019

> **Auro Pharmacies Inc. DBA Central Drugs** · Class III · drug recall initiated 2019-03-22.

## 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.

## Distribution

Nationwide within the United States

## Key facts

- **Recall number:** D-1082-2019
- **Recalling firm:** Auro Pharmacies Inc. DBA Central Drugs
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2019-03-22
- **Report date:** 2019-04-17
- **Termination date:** 2020-02-27

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** La Habra, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1082-2019

## Citation

> AI Analytics. FDA recall D-1082-2019. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/D-1082-2019. Source: US FDA. Licensed CC0.

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