Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:27803
Brand Name:Bard Australia - Iliofemoral vein stent
Model:
Affected:All codes and lots of VENOVO Venous Stent System
Software version:
Recalling Organisation:Pharmacy Retailing (NZ) Ltd t/a Healthcare Logistics
54 Carbine Road
Mt Wellington
AUCKLAND
Contact Information:09 969 0705
Manufacturer:Angiomed GmbH & Co. Medizintechnik KG
Issue:The manufacturer recently confirmed reports on the VENOVO Venous Stent System where the proximal end of the stent does not immediately expand upon deployment. The proximal end of the stent remains connected to the delivery system.
Recall action type:Recall
Recall action:Product to be returned to supplier
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:28/5/2021
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