Type of Product |
Medical Device |
TGA Recall Reference |
RC-2017-RN-00475-1 |
Product Name/Description |
Corpuls3 defibrillator/monitoring unit – Printer Paper
Product Code: CP-4121
Batch Numbers: D447, D465
ARTG Number: 192745 |
Recall Action Level |
Hospital |
Recall Action Classification |
Class III |
Recall Action Commencement Date |
10/04/2017 |
Responsible Entity |
|
Reason/Issue |
Corpuls has been notified of some batches of Corpuls3 Printer Paper where the paper manufacturer has applied too much glue to the sides. The applied glue prevents the paper from proper rolling out. Only a few roles in a pack may be affected. |
Recall Action |
Recall |
Recall Action Instructions |
Device Technologies is advising users to quarantine and dispose of all affected stock. Replacement stock will be provided. This action has been closed-out on 06/07/2017. |
Contact Information |
02 9972 8353 - Device Technologies |