Z-0645-2013 Class II Terminated

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

Recall Details

Product Type
Devices
Report Date
January 16, 2013
Initiation Date
September 20, 2012
Termination Date
March 12, 2013
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
10 units

Product Description

ABX PENTRA ML, Software Versions: V8.0.x and Below; V.9.0.1 and V9.0.2

Reason for Recall

Horiba Medical is recalling ABX PENTRA ML because they have confirmed an issue with the ABX PENTRA ML data management and validation system. An incorrect patient result is transmitted to the Laboratory Information System. This result is from a previous run of the same patient that is stored in the ML database. This issue occurs in a very rare sequence of specific events. The affected software

Distribution Pattern

Nationwide in the US, including the states of CA, MI, IN, FL, and GA. Center Recall Depth is Retail.

Code Information

Lot/Serial# PML0937