FDA Recall Terminated

Device Name: ABX PENTRA ML Model/Part #(s): A11A01652 Lot/Serial #(s): N/A Software Version(s): All versions are subject to this correction. Product Usage: The ABX PENTRA ML is a software data management system intended for use on ABX Hematology Analyzers.

Recall: Z-1173-2014 · Initiated February 14, 2014

Recall

Recall Number
Z-1173-2014
Event Number
67528
Firm
Horiba Instruments, Inc dba Horiba Medical
FEI Number
3002698356
Product Code
JQP
Status
Terminated
Root Cause
Software design
Initiated
February 14, 2014
Posted
March 11, 2014
Terminated
August 22, 2014
Address
34 Bunsen, Irvine, CA, 92618-4210

Description

Device Name: ABX PENTRA ML Model/Part #(s): A11A01652 Lot/Serial #(s): N/A Software Version(s): All versions are subject to this correction. Product Usage: The ABX PENTRA ML is a software data management system intended for use on ABX Hematology Analyzers.

Reason

HORIBA Medical initiated this recall of all software versions of ABX PENTRA ML (Model A11A06152) due to a software bug with the potential of transmitting incorrect results to the Laboratory Information System.

Action

Horiba sent an "URGENT SAFETY NOTICE letter datedFebruary 13, 2014 via by mail to customers. The letter identified the affected product, issue, impact, actions to be taken. Customers were instructed to share this information with laboratory staff and retain this notification as part of their laboratory documentation. Customers were requested to complete and return the enclosed response form via one of the following methods: Fax: 949-453-0600 Email: [email protected] Mail: HORIBA Medical Attention: Jim Knowles, Recall Coordinator 34 Bunsen Drive Irvine, CA 92618. For questions contact your local Horiba Medical representative.

Distribution

USA Nationwide Distribution

Quantity

15