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.
FDA Recall Z-1173-2014 · Posted 2014-03-11
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Recalling FirmHoriba Instruments, Inc dba Horiba Medical
Recall StatusTerminated
Product CodeJQP
Date Initiated2014-02-14
Date Terminated2014-08-22
Product Quantity15
Reason for Recall
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.
Firm 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.
Root Cause
Software design
Distribution Pattern
USA Nationwide Distribution
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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