# FDA recall D-0668-2016

> **Hospira Inc.** · Class I · drug recall initiated 2016-01-05.

## Product

Magnesium Sulfate in Water for Injection, (0.325 mEq Mg++/mL) 40 mg/mL, 2 g Total, 50 mL Single-Dose Container bag, Hospira, Inc., Lake Forest, IL  60045, NDC 0409-6729-24.

## Reason for recall

Labeling: Incorrect Barcode: Primary bag labeling may be mislabeled with the wrong barcode which scans in as heparin sodium.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0668-2016
- **Recalling firm:** Hospira Inc.
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2016-01-05
- **Report date:** 2016-02-24
- **Termination date:** 2017-09-28

- **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-0668-2016

## Citation

> AI Analytics. FDA recall D-0668-2016. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-0668-2016. Source: US FDA. Licensed CC0.

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