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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 Baxter Healthcare Pty Ltd
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