Zenzedi — Class I drug recall D-0323-2024
Terminated recall by Azurity Pharmaceuticals, Inc., reported 2024-02-07, distributed nationwide. Labeling: Label Mix-up
| Recall number | D-0323-2024 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Azurity Pharmaceuticals, Inc., Wilmington, MA, United States |
| Recall initiated | 2024-01-04 |
| Classified | 2024-02-12 |
| Reported by FDA | 2024-02-07 |
| Terminated | 2024-09-18 |
| Distributed | Nationwide (US) |
| Quantity | 4,662 bottles |
| Reason classes | labeling |
| NDC | 24338-0850, 24338-0850-03, 24338-0851, 24338-0851-03, 24338-0852, 24338-0852-03, 24338-0853, 24338-0853-03, 24338-0854, 24338-0854-03, 24338-0855, 24338-0855-03, 24338-0856, 24338-0856-03 |
| Lot numbers | F230169A |
| Expiration dates | 2025-06-30 |
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
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-0323-2024. 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.