Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:20717
Brand Name:Endologix Nellix Endovascular Sealing System
Model:
Affected:Nelix 3SQ+
Software version:
Recalling Organisation:eVas Medical
73 Churchill Road
Murrays Bay
Auckland 0630
Contact Information:
Manufacturer:Endologix LLC
Issue:The manufacturer will be updating the IFU with more detailed information regarding the indications for use, patient selection criteria, and procedural best practices for the EndoVascular Aneurysm Sealing System.
Recall action type:Correction
Recall action:Instructions for use to be updated
Level of recall:Healthcare Professional
Date Commenced:13/10/2016
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