# FDA recall Z-2675-2017

> **ICU** · Class II · device recall initiated 2013-02-01.

## Product

The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self contained, microprocessor based infusion devices. The pumps are available in single channel and in triple channel pumping mechanism types.

## Reason for recall

A possible interruption of therapy when an E321 error code occurs while using the infuser, which is caused by battery issues.

## Distribution

Nationwide, Worldwide

## Key facts

- **Recall number:** Z-2675-2017
- **Recalling firm:** ICU
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2013-02-01
- **Report date:** 2017-07-19
- **Termination date:** 2018-05-31

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2675-2017

## Citation

> AI Analytics. FDA recall Z-2675-2017. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/Z-2675-2017. Source: US FDA. Licensed CC0.

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