fentaNYL Citrate 2 — Class II drug recall D-0432-2024
Ongoing recall by IntegraDose Compounding Services LLC, reported 2024-04-10, distributed nationwide. Lack of Assurance of Sterility: leaking bags
| Recall number | D-0432-2024 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | IntegraDose Compounding Services LLC, Minneapolis, MN, United States |
| Recall initiated | 2024-03-22 |
| Classified | 2024-04-03 |
| Reported by FDA | 2024-04-10 |
| Distributed | Nationwide (US) |
| Quantity | 187 cassettes |
| Reason classes | sterility, packaging |
| NDC | 71139-6030-01 |
| Lot numbers | 20231020FEN-1 |
| Expiration dates | 2024-04-17 |
Product
fentaNYL Citrate 2,500 mcg/50mL in Sterile Water, 50 mL CADD for Injection, IntegraDose Compounding Services, LLC, 719 Kasota Ave SE, Minneapolis, MN. NDC 71139-6030-1
Reason for recall
Lack of Assurance of Sterility: leaking bags
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-0432-2024. 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.