Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:18190
Brand Name:Endologix Nellix EndoVascular Aneurysm Sealing System
Model:All models
Affected:All lots
Software version:
Recalling Organisation:eVas Medical
73 Churchill Road
Murrays Bay
Auckland 0630
Contact Information:
Manufacturer:Endologix LLC
Issue:The manufacturer is updating the instructions for use to include new safety information.
* It is mandatory to perform the EndoBag pre-fill step
* Use only non-heparinised sterile saline for the EndoBag prer-fill step
* After aspiration of the pre-fill non-heparinised sterile sale volume, carefully inject polymer solution into the EndoBags under pressure monitoring
Recall action type:Correction
Recall action:Instructions for use to be updated
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:17/3/2015
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