# FDA recall D-0293-2015

> **Baxter Healthcare Corp.** · Class II · drug recall initiated 2014-04-24.

## Product

Famotidine Injection 20 mg, Rx Only, GALAXY Single Dose Container, Code 2G3424, Sterile Nonpyrogenic, 50 mL Iso-osmotic,  Baxter Healthcare Corporation, Deerfield, IL 60015, USA, NDC 0338-5197-41.

## Reason for recall

Presence of Particulate Matter: Baxter Healthcare Corporation has received a complaint reporting the presence of particulate matter identified as plastic/rubber in famotidine Injection premixed containers.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0293-2015
- **Recalling firm:** Baxter Healthcare Corp.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-04-24
- **Report date:** 2014-12-17
- **Termination date:** 2015-06-16

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Deerfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0293-2015

## Citation

> AI Analytics. FDA recall D-0293-2015. Retrieved 2026-05-24 from https://api.ai-analytics.org/recall/D-0293-2015. Source: US FDA. Licensed CC0.

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