Z-0645-2013 Class II Terminated
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