Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:18948
Brand Name:Siemens RapidPoint 500 System
Model:10492730, 10696855, 10696857, 10697306
Affected:All units
Software version:
Recalling Organisation:Siemens Healthcare (NZ) Ltd
55 Hugo Johnston Drive
Penrose
Auckland
Contact Information:0800 310 300
Manufacturer:Siemens Healthcare Diagnostics Inc
Issue:When both ports (Serial and Ethernet) are configured to transmit data, the data stream from one port could potentially affect the data stream from the other port.
This could cause the message received by the LIS (data management system) to include either
* Duplicate data
* Missing data
* Data from a different patient.
Siemens has not observed this scenario and the expected frequency of occurrence is extremely unlikely.
If this issue occurs, only one analyte has the potential to be affected (i.e. if a panel of analytes is ordered, only one could be affected).
Recall action type:Correction
Recall action:Software to be upgraded
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:3/8/2015
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