Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 25524 |
| Brand Name: | Gore_Excluder AAA Contralateral Leg Endoprosthesis (Codes PLC & PXC) |
| Model: | GORE EXCLUDER AAA |
| Affected: | |
| Software version: | |
| Recalling Organisation: | InterMed Medical Ltd 71 Apollo Drive Albany AUCKLAND 1311 |
| Contact Information: | 0800 333 444 |
| Manufacturer: | W L Gore & Associates Inc |
| Brand Name: | Gore_Excluder AAA Trunk Ipsilatral Leg Endoprosthesis (Codes RLT & RMT) |
| Model: | GORE EXCLUDER Iliac |
| Affected: | |
| Software version: | |
| Recalling Organisation: | InterMed Medical Ltd 71 Apollo Drive Albany AUCKLAND 1311 |
| Contact Information: | 0800 333 444 |
| Manufacturer: | W L Gore & Associates Inc |
| Issue: | The manufacturer has received reports of leading end catheter component separations of the EXCLUDER Device. Of the events, 30 reported immediate health consequences and 1 long-term health consequence (pelvic ischemia). This represents a rate of 0.05% reported complaints of leading end catheter separation events over the last 6 years . Based on these events, Gore will be updating its Instructions for Use. |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 7/1/2020 |
