FDA Drug recall D-0323-2024
Zenzedi (Dextroamphetamine Sulfate) CII Tablets, USP, 30 mg, 30-count bottle, Rx only, Mfd. for: Arbor Pharmaceuticals, LLC., Atlanta, Geor…
- FDA Drug
- Class I
- terminated
- Published 2024-02-07
On 2024-02-07 the FDA classified a Class I recall of Zenzedi (Dextroamphetamine Sulfate) CII Tablets, USP, 30 mg, 30-count bottle, Rx only, Mfd. for: Arbor Pharmaceuticals, LLC., Atlanta, Geor… by Azurity Pharmaceuticals, citing labeling: Label Mix-up.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0323-2024 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2024-01-04 |
| Published | 2024-02-07 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Azurity Pharmaceuticals |
| Distribution | US |
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
Labeling: Label Mix-up
Identifiers
| ndc | 24338-850-03 |
|---|---|
| ndc | 24338-851-03 |
| ndc | 24338-852-03 |
| ndc | 24338-853-03 |
| ndc | 24338-854-03 |
| ndc | 24338-855-03 |
| ndc | 24338-856-03 |
| code_info | Lot # F230169A, Exp. 06/30/2025 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0323-2024%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.