Fentanyl Citrate 2 mcg per mL — Class II drug recall D-0334-2019
Terminated recall by Pharmedium Services, LLC, reported 2018-12-26, distributed nationwide. Sub-potent
| Recall number | D-0334-2019 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Pharmedium Services, LLC, Lake Forest, IL, United States |
| Recall initiated | 2018-12-05 |
| Classified | 2018-12-15 |
| Reported by FDA | 2018-12-26 |
| Terminated | 2020-10-02 |
| Distributed | Nationwide (US) |
| Quantity | 295 |
| Reason classes | potency |
| NDC | 61553-0148-48 |
| Lot numbers | 183230004C |
| Expiration dates | 2019-02-17 |
Product
Fentanyl Citrate 2 mcg per mL (200 mcg per 100 mL) and Ropivacaine HCl 0.2% in Sodium Chloride 0.9%, Injection, 100 mL total volume in a 150 mL Intravia Bag, Rx Only,PharMEDium Services, LLC. 913 N. Davis Ave. Cleveland, MS 38732. NDC 61553-148-48
Reason for recall
Sub-potent
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-0334-2019. 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.