MAGNESIUM SULFATE IN 5% DEXTROSE INJECTION — Class I drug recall D-1076-2015
Terminated recall by Hospira Inc., reported 2015-05-20, distributed nationwide. Labeling: Wrong Bar Code: There is a potential for some units to be mislabeled with an incorrect barcode on th
| Recall number | D-1076-2015 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hospira Inc., Lake Forest, IL, United States |
| Recall initiated | 2015-03-06 |
| Classified | 2015-05-13 |
| Reported by FDA | 2015-05-20 |
| Terminated | 2016-10-19 |
| Distributed | Nationwide (US) |
| Quantity | 181,704 bags |
| Reason classes | labeling |
| NDC | 00409-6727, 00409-6727-11, 00409-6727-23, 00409-6727-24, 00409-6727-55 |
| Lot numbers | 42-120-JT |
| Expiration dates | 2015-12-01 |
Product
MAGNESIUM SULFATE IN 5% DEXTROSE INJECTION, USP, 10 mg/mL; 100 mL bag, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-6727-23, UPC (01) 0 030409 672723 1.
Reason for recall
Labeling: Wrong Bar Code: There is a potential for some units to be mislabeled with an incorrect barcode on the immediate container that scans as heparin sodium 2000 USP units/1000 mL in 0.9% in sodium chloride injection.
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-1076-2015. 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.