Z-0493-2018 Class II Terminated

Recalled by Horiba Instruments, Inc dba Horiba Medical — Irvine, CA

Recall Details

Product Type
Devices
Report Date
February 7, 2018
Initiation Date
November 21, 2017
Termination Date
November 4, 2019
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
10 bags, 100 units each

Product Description

10 ML REAGENT CUP, B1034626, SAP 1221034626 for use with ABX PENTRA 400 / PENTRA C400

Reason for Recall

The ABX PENTRA Reagent Containers do not always sit properly into the reagent rack. In low reagent level scenarios, this could lead to insufficient reagent volume being pipetted and could lead to incorrect results being reported without an alarm.

Distribution Pattern

Nationwide

Code Information

DATE - MVT 25.08.2017