# FDA recall D-1390-2012

> **Hospira, Inc.** · Class III · drug recall initiated 2012-04-05.

## Product

Magnesium Sulfate in Water for Injection, 40 mg/mL (0.325 mEq Mg++/mL), 2 g total, 50 mL Flexible Container, Rx only, Hospira, Inc., Lake Forest, IL 60045; NDC 0409-6729-24.

## Reason for recall

Superpotent (Single Ingredient) Drug: Above specification assay results for percentage of magnesium sulfate.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1390-2012
- **Recalling firm:** Hospira, Inc.
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2012-04-05
- **Report date:** 2012-06-27
- **Termination date:** 2013-08-08

- **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-1390-2012

## Citation

> AI Analytics. FDA recall D-1390-2012. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-1390-2012. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*