# FDA recall Z-2671-2017

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

## Product

Alaris PC Unit, Model 8015

## Reason for recall

BD initiated the recall of Alaris PC unit model 8015 after the firm identified five scenarios which can result in the occurrence of Systems Error Code 255-16-275 and can potentially result in interrupted infusions.

## Distribution

Worldwide Distribution - USA (nationwide) and to the countries of :  Europe, Australia, New Zealand,  South Africa, Greater Asia, Middle East, and Canada.

## Key facts

- **Recall number:** Z-2671-2017
- **Recalling firm:** CareFusion 303, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-06-12
- **Report date:** 2017-07-12
- **Termination date:** 2018-10-26

- **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-2671-2017

## Citation

> AI Analytics. FDA recall Z-2671-2017. Retrieved 2026-06-30 from https://api.ai-analytics.org/recall/Z-2671-2017. Source: US FDA. Licensed CC0.

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