Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:21090
Brand Name:StarClose SE Vascular Closure System
Model:
Affected:50831K1, 50903K1, 50911K1,50921K1, 50924K1, 50929K1, 51002K1, 51008K1, 51016K1, 51026K1, 51029K1,51103K1
Software version:
Recalling Organisation:Abbott Vascular Division of Abbott Laboratories (NZ) Ltd
Ground Floor, Building D
4 Pacific Rise
Mount Wellington
Auckland 1060
Contact Information:0800 827 285
Manufacturer:Abbott Vascular (USA)
Issue:Product may exhibit difficulty or failure to deploy the StarClose SE Clip. Potential risks associated with this event include prolonged procedure times, use of another device or manual compression to achieve hemostasis.
Recall action type:Recall
Recall action:Product to be returned to supplier
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:9/2/2017
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