# FDA recall Z-0236-2018

> **Beckman Coulter Inc.** · Class II · device recall initiated 2017-11-03.

## Product

UniCel DxH800, Part Numbers:  629029 and B24802,  automated hematology analyzer

## Reason for recall

The shield for the Single-Tube Station on the DxH instrument may interfere with sample aspiration in the open vial position.

## Distribution

CA, AR, HI, CA, OH, WA, MD, Canada, Japan

## Key facts

- **Recall number:** Z-0236-2018
- **Recalling firm:** Beckman Coulter Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-11-03
- **Report date:** 2017-12-20
- **Termination date:** 2018-06-19

- **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-0236-2018

## Citation

> AI Analytics. FDA recall Z-0236-2018. Retrieved 2026-06-08 from https://api.ai-analytics.org/recall/Z-0236-2018. Source: US FDA. Licensed CC0.

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