FDA Drug recall D-1076-2015
MAGNESIUM SULFATE IN 5% DEXTROSE INJECTION, USP, 10 mg/mL
- FDA Drug
- Class I
- terminated
- Published 2015-05-20
On 2015-05-20 the FDA classified a Class I recall of MAGNESIUM SULFATE IN 5% DEXTROSE INJECTION, USP, 10 mg/mL by Hospira, citing 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/100….
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1076-2015 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2015-03-06 |
| Published | 2015-05-20 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Hospira |
| Distribution | US |
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
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.
Identifiers
| ndc | 0409-6727-11 |
|---|---|
| ndc | 0409-6727-23 |
| ndc | 0409-6727-55 |
| ndc | 0409-6727-24 |
| code_info | Lot: 42-120-JT, Exp 01DEC2015 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1076-2015%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.