# FDA recall Z-2700-2017

> **CareFusion 303, Inc.** · Class II · device recall initiated 2017-06-12.

## Product

Alaris Pump Module model 8100

## Reason for recall

There is a potential risk that could cause unintended flow in the older, centered sear door latch design in the Alaris Pump module model 8100.

## Distribution

US and Canada

## Key facts

- **Recall number:** Z-2700-2017
- **Recalling firm:** CareFusion 303, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-06-12
- **Report date:** 2017-07-19
- **Termination date:** 2019-01-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** San Diego, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2700-2017

## Citation

> AI Analytics. FDA recall Z-2700-2017. Retrieved 2026-07-11 from https://api.ai-analytics.org/recall/Z-2700-2017. Source: US FDA. Licensed CC0.

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