Type of Product |
Medical Device |
TGA Recall Reference |
RC-2014-RN-01199-1 |
Product Name/Description |
HomeChoice PRO Automated PD System Automated PD System Devices
Product Code: R5C8320
ARTG number: 172780 |
Recall Action Level |
Hospital |
Recall Action Classification |
Class II |
Recall Action Commencement Date |
20/11/2014 |
Responsible Entity |
|
Reason/Issue |
Baxter Healthcare Corporation is sending this communication to inform users of additional and updated warnings and cautions that are not in the Patient At-Home Guide. |
Recall Action |
Recall for Product Correction |
Recall Action Instructions |
Baxter is notifying clinicians and home use patients of the additional and updated warnings and cautions that are not in the Patient At-Home Guide. This action has been closed-out on 06/07/2016. |
Contact Information |
1300 789 646 - Baxter Healthcare Customer Service |