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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 Device Technologies Australia Pty Ltd
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