# FDA recall D-1076-2015

> **Hospira Inc.** · Class I · drug recall initiated 2015-03-06.

## 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.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1076-2015
- **Recalling firm:** Hospira Inc.
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-03-06
- **Report date:** 2015-05-20
- **Termination date:** 2016-10-19

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Lake Forest, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1076-2015

## Citation

> AI Analytics. FDA recall D-1076-2015. Retrieved 2026-05-29 from https://api.ai-analytics.org/recall/D-1076-2015. Source: US FDA. Licensed CC0.

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