| 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 |
|
| 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 |