# FDA recall D-0323-2024

> **Azurity Pharmaceuticals, Inc.** · Class I · drug recall initiated 2024-01-04.

## Product

Zenzedi (Dextroamphetamine Sulfate) CII Tablets, USP, 30 mg, 30-count bottle, Rx only, Mfd. for: Arbor Pharmaceuticals, LLC., Atlanta, Georgia, 30328, NDC 24338-856-03

## Reason for recall

Labeling: Label Mix-up

## Distribution

USA nationwide

## Key facts

- **Recall number:** D-0323-2024
- **Recalling firm:** Azurity Pharmaceuticals, Inc.
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2024-01-04
- **Report date:** 2024-02-07
- **Termination date:** 2024-09-18

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Wilmington, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0323-2024

## Citation

> AI Analytics. FDA recall D-0323-2024. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/D-0323-2024. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*