Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 21973 |
| Brand Name: | Endologix Nellix Endovascular Sealing System |
| Model: | |
| Affected: | changes to the Nellix IFU |
| Software version: | |
| Recalling Organisation: | Endologix New Zealand Co. Level 27 88 Shortland Street Auckland 1010 |
| Contact Information: | |
| Manufacturer: | Endologix International BV |
| Issue: | Nellix IFU has been updated with additional information related to secondary interventions in patients who have specific Nellix related complications, and information related to off-label use of the Nellix System. |
| Recall action type: | Correction |
| Recall action: | |
| Level of recall: | |
| Date Commenced: | 14/9/2017 |
