Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 24099 |
| Brand Name: | Endologix Nellix Endovascular Sealing System (3.5 and 3SQ) |
| Model: | Nellix EndoVascular Aneurysm Sealing System - Component - Nellix Accessory Kit, Nellix Dispenser – Reusable, Nellix Dispenser – Disposable, Nellix Polymer |
| Affected: | |
| Software version: | |
| Recalling Organisation: | Endologix New Zealand Co. Level 27 88 Shortland Street Auckland 1010 |
| Contact Information: | |
| Manufacturer: | Endologix International BV |
| Issue: | The manufacturer is ceasing sales, effective immediately, and requesting the return of all unused Nellix Systems due to adverse events including migration, Type 1 endoleak, and aneurysm enlargement, which the manufacturer predominately attributes to use outside of the current indications. |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Wholesale |
| Date Commenced: | 24/1/2019 |
