ePHEDrine Sulfate In 0 — Class II drug recall D-0220-2018
Terminated recall by Pharmedium Services, LLC, reported 2018-01-24, distributed nationwide. Subpotent Drug
| Recall number | D-0220-2018 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Pharmedium Services, LLC, Lake Forest, IL, United States |
| Recall initiated | 2017-10-30 |
| Classified | 2018-01-12 |
| Reported by FDA | 2018-01-24 |
| Terminated | 2020-05-07 |
| Distributed | Nationwide (US) |
| Quantity | 5,002 syringes |
| Reason classes | potency |
| NDC | 71030-0003-10, 71030-0003-12, 71030-0003-20, 71030-0003-21 |
| Lot numbers | 172840015D, 172840176M, 172880044M, 172920115M, 172930139M, 172940003M, 172950036M |
| Expiration dates | 2018-01-10, 2018-01-11, 2018-01-14, 2018-01-18, 2018-01-19, 2018-01-20, 2018-01-21 |
Product
ePHEDrine Sulfate In 0.9% Sodium Chloride, 5 mg per mL (50 mg per 10 mL), 10 mL Total Volume pre-filled syringes, packaged in a) 5-count cartons, NDC 71030-0003-10 and NDC 71030-0003-20, and b) 25-count cartons, NDC 71030-0003-21 and NDC 71030-0003-12, Rx Only, PharMEDium Services, LLC, 913 N. Davis Ave, Cleveland, MS, Code 2R3304.
Reason for recall
Subpotent Drug
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-0220-2018. 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.