morphine sulfate 1 mg per mL in 0 — Class II drug recall D-0999-2017
Terminated recall by SCA Pharmaceuticals, reported 2017-08-02, distributed nationwide. Lack of Assurance of Sterility: Product made with recalled 0.9% sodium chloride bags which have the potential
| Recall number | D-0999-2017 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | SCA Pharmaceuticals, Little Rock, AR, United States |
| Recall initiated | 2017-07-14 |
| Classified | 2017-07-25 |
| Reported by FDA | 2017-08-02 |
| Terminated | 2019-10-30 |
| Distributed | Nationwide (US) |
| Quantity | 220 bags |
| Reason classes | sterility, packaging |
| NDC | 70004-0100-58, 70004-0100-59 |
| Expiration dates | 2017-10-04, 2017-10-05, 2017-10-08 |
Product
morphine sulfate 1 mg per mL in 0.9% Sodium Chloride, (Total morphine Dose 100 mg/100 mL), Total Volume 100 mL Single Dose Container bag, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct, Little Rock, AR 72205, (877) 550-5059; labeled as a) NDC: 70004-0100-59; b) NDC: 70004-100-58.
Reason for recall
Lack of Assurance of Sterility: Product made with recalled 0.9% sodium chloride bags which have the potential to leak.
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-0999-2017. 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.