Beckman Coulter Inc.: Medical Device Recall in 2017 - (Recall #: Z-0236-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: November 3, 2017

Date Posted: December 20, 2017

Recall Number: Z-0236-2018

Event ID: 78611

Reason for Recall:

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

Status: Terminated

Product Quantity: 15 units

Code Information:

Serial Numbers: B24802: AW10161, AW10154, AZ34449, AZ34447 629029: AT40563, AT06096, AT06095, AT02044, AW05080, AW05072, AW05066, AT50679, AS49422, AS36312, AS23151

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated