Duloxetine Delayed-Release Capsules — Class II drug recall D-0277-2025
Ongoing recall by Rising Pharma Holding, Inc., reported 2025-03-26, distributed nationwide. CGMP Deviations: Presence of N-nitroso-duloxetine impurity above recommended interim limit.
| Recall number | D-0277-2025 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Rising Pharma Holding, Inc., East Brunswick, NJ, United States |
| Recall initiated | 2025-03-05 |
| Classified | 2025-03-14 |
| Reported by FDA | 2025-03-26 |
| Distributed | Nationwide (US) |
| Quantity | 1,223 bottles |
| Reason classes | cgmp, specification failure |
| NDC | 57237-0018-99 |
| Lot numbers | DTB23111A |
| Expiration dates | 2025-08-31 |
Product
Duloxetine Delayed-Release Capsules, USP, 30 mg, 1,000-count bottle, Rx only, Distributed by: Rising Health, LLC, Saddle Brook, NJ 07663, NDC 57237-018-99
Reason for recall
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above recommended interim limit.
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-0277-2025. 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.