# FDA recall D-0123-2018

> **Pfizer Inc.** · Class I · drug recall initiated 2017-08-30.

## Product

Vancomycin Hydrochloride for Injection, USP. 750 mg.  Sterile Powder. Rx Only. Hospira, Inc., Lake Forest, IL 60045 USA.  NDC:  0409-6531-02

## Reason for recall

Presence of Particulate Matter: glass particulate found in vial

## Distribution

Nationwide USA and Puerto Rico

## Key facts

- **Recall number:** D-0123-2018
- **Recalling firm:** Pfizer Inc.
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2017-08-30
- **Report date:** 2017-12-27
- **Termination date:** 2018-11-08

- **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-0123-2018

## Citation

> AI Analytics. FDA recall D-0123-2018. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-0123-2018. Source: US FDA. Licensed CC0.

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