# FDA recall D-1232-2015

> **Hospira Inc.** · Class III · drug recall initiated 2015-05-19.

## Product

Magnesium Sulfate Injection, USP, 50%, 20mL, Single dose Fliptop Vial, For IV or IM use, Rx only, Manufactured  by Hospira, Inc. 4285 Wesleyan Blvd Rocky Mount, NC 27804 for Hospira, Inc. 275 N Field Drive, Lake Forest, IL 60045. NDC 0409-2168-02

## Reason for recall

Failed pH Specifications: 12 month stability testing

## Distribution

U.S. Nationwide, Kuwait, Bahrain and Israel.

## Key facts

- **Recall number:** D-1232-2015
- **Recalling firm:** Hospira Inc.
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-05-19
- **Report date:** 2015-07-15
- **Termination date:** 2017-12-04

- **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-1232-2015

## Citation

> AI Analytics. FDA recall D-1232-2015. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-1232-2015. Source: US FDA. Licensed CC0.

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