FentaNYL Citrate 2 — Class II drug recall D-0078-2023
Terminated recall by OurPharma LLC, reported 2022-12-21, distributed in MO. Underfilled units.
| Recall number | D-0078-2023 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | OurPharma LLC, Fayetteville, AR, United States |
| Recall initiated | 2022-11-29 |
| Classified | 2022-12-09 |
| Reported by FDA | 2022-12-21 |
| Terminated | 2024-09-20 |
| Distributed | MO |
| Quantity | 691 cassettes |
| NDC | 73013-0001-01 |
| Lot numbers | 100122060007, 100122060008, 100122070002 |
| Expiration dates | 2022-12-17, 2022-12-18, 2023-01-09 |
Product
FentaNYL Citrate 2.5 mg/50 mL (50mcg/ml) Injection Solution, Preservative Free, Single Use 50 ml Cassette, Rx Only, Repackaged by OurPharma, LLC. 2512 S. City Lake Rd. Fayetteville, AR 72701, 1-833-290-2654, NDC 73013-001-01
Reason for recall
Underfilled units.
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-0078-2023. 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.