# FDA recall D-0015-2019

> **Pfizer Inc.** · Class II · drug recall initiated 2018-10-03.

## Product

Magnesium Sulfate in Water for Injection (0.325 mEq Mg++/mL) 40 mg/mL, 20 g Total, 500 mL Single-Dose Container bag, Rx only, Hospira, Inc. Lake Forest, IL 60045 USA, NDC 0409-6729-03.

## Reason for recall

Correct Labeled Product Mispack: confirmed report involving a single unit of properly labeled Heparin in 0.45% Sodium Chloride for Injection (NDC 0409-7651-03, Lot 87903FW) that was found inside a case of Magnesium Sulfate in Water for Injection.

## Distribution

Nationwide in the USA and Puerto Rico

## Key facts

- **Recall number:** D-0015-2019
- **Recalling firm:** Pfizer Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2018-10-03
- **Report date:** 2018-10-17
- **Termination date:** 2020-10-02

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** New York, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0015-2019

## Citation

> AI Analytics. FDA recall D-0015-2019. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/D-0015-2019. Source: US FDA. Licensed CC0.

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