# FDA recall Z-2690-2017

> **Beckman Coulter Inc.** · Class II · device recall initiated 2017-05-22.

## Product

Coulter PrepPlus 2, Part Number 378600,     Product Usage:  The COULTER PrepPlus 2, when used in combination with the COULTER TQPrep Workstation, is intended to prepare human whole blood for In Vitro Diagnostic (IVD) Use with cleared Beckman Coulter IVD applications on cleared Beckman Coulter flow cytometers (FC500, Navios and Navios EX). The COULTER PrepPlus 2 is a microprocessor-controlled pipetting and diluting system, designed for automating sample preparation or assay methods. It is capable of aspirating and dispensing liquid samples.

## Reason for recall

When samples are prepared using the PrepPlus or PrepPlus 2 sample preparation systems and then run on a Flow cytometer, there is an imprecision in the absolute counts on only the first tube in a run.

## Distribution

Worldwide Distribution

## Key facts

- **Recall number:** Z-2690-2017
- **Recalling firm:** Beckman Coulter Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-05-22
- **Report date:** 2017-07-12
- **Termination date:** 2021-03-31

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2690-2017

## Citation

> AI Analytics. FDA recall Z-2690-2017. Retrieved 2026-07-13 from https://api.ai-analytics.org/recall/Z-2690-2017. Source: US FDA. Licensed CC0.

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