Print version of this report
Type of Product Medical Device
TGA Recall Reference RC-2012-RN-00811-3
Product Name/Description Surecan Safety II (Needles with special bevel for implanatable access ports).

Product codes: 4447033, 4447034, 4447035 and 4447036
Recall Action Level Hospital
Recall Action Classification Class II
Recall Action Commencement Date 30/08/2012
Responsible Entity B Braun Australia Pty Ltd
Reason/Issue Due to an administrative system failure identified within the company, the product, not currently approved for inclusion in the Australian Register of
Therapeutic Goods (ARTG), has been inadvertently distributed to hospitals.
Recall Action Recall
Recall Action Instructions Quarantine and return affected product to B. Braun
Contact Information 1800 251 705 - B.Braun Recall Coordinator