Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 23746 |
| Brand Name: | Endologix Nellix Endovascular Sealing System (3SQ+ and 3.5) |
| Model: | N10-100, N10-130, N10-140, N10-160, N10-170, N10-180, N10-200 |
| Affected: | Item #s : F00479, F00735, F00480, F00736, F00481, F00737, F00482, F00738, F00483 and F00515 |
| Software version: | |
| Recalling Organisation: | Endologix New Zealand Co. Level 27 88 Shortland Street Auckland 1010 |
| Contact Information: | |
| Manufacturer: | Endologix International BV |
| Issue: | The manufacturer has identified additional factors linked to the adequacy of the technical procedure that may place patients at higher risk of experiencing a Nellix-related complication. |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Healthcare Professional |
| Date Commenced: | 24/10/2018 |
