Ephedrine sulfate 5 mg/mL in 0 — Class II drug recall D-0156-2018
Terminated recall by SCA Pharmaceuticals, reported 2018-01-17, distributed nationwide. Labeling: Incorrect or Missing Lot and/or Exp Date - product label was missing lot number and beyond use date.
| Recall number | D-0156-2018 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | SCA Pharmaceuticals, Little Rock, AR, United States |
| Recall initiated | 2017-12-07 |
| Classified | 2018-01-05 |
| Reported by FDA | 2018-01-17 |
| Terminated | 2019-05-01 |
| Distributed | Nationwide (US) |
| Quantity | 1,248 syringes |
| Reason classes | labeling |
| NDC | 70004-0600-12 |
| Expiration dates | 2017-12-27 |
Product
Ephedrine sulfate 5 mg/mL in 0.9% Sodium Chloride 10 mL in Single Dose Syringe, Total Volume 10 mL, Rx only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC 70004-0600-12
Reason for recall
Labeling: Incorrect or Missing Lot and/or Exp Date - product label was missing lot number and beyond use date.
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-0156-2018. 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.