# FDA recall D-0136-2020

> **Pfizer Inc.** · Class II · drug recall initiated 2019-10-02.

## Product

10% LMD in 5% Dextrose Injection Dextran 40 in Dextrose Injection, USP,  500 mL bags, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7418-13

## Reason for recall

Lack of Assurance of Sterility:  Bag has the potential to leak.

## Distribution

Nationwide in the United States and Puerto Rico

## Key facts

- **Recall number:** D-0136-2020
- **Recalling firm:** Pfizer Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2019-10-02
- **Report date:** 2019-10-16
- **Termination date:** 2020-12-01

- **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-0136-2020

## Citation

> AI Analytics. FDA recall D-0136-2020. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-0136-2020. Source: US FDA. Licensed CC0.

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