Print version of this report
Type of Product Medical Device
TGA Recall Reference RC-2012-RN-00869-3
Product Name/Description ADVIA Centaur and ADVIA Centaur XP (Immuno-assay analysers). An in vitro diagnostic medical device (IVD)

ARTG Number: 174383
Recall Action Level Hospital
Recall Action Classification Class II
Recall Action Commencement Date 31/08/2012
Responsible Entity Siemens Ltd Diagnostics Division
Reason/Issue Siemens Healthcare Diagnostics has determined that a small amount of residual cleaning solution may remain in the system fluidic lines following the Monthly Cleaning Procedure (MCP) and the Daily Cleaning Procedure (DCP).
Recall Action Recall for Product Correction
Recall Action Instructions Siemens is providing work around instructions for users to follow.
Contact Information 1800 310 300 - Siemens Technical Support Centre