Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 26654 |
| Brand Name: | Stryker Neurovascular - III - 58173 - Embolectomy/thrombectomy suction catheter |
| Model: | Trevo® XP ProVue Retriever 4MM x 20MM, Trevo® XP ProVue Retriever 4MM x 30MM, Trevo® XP ProVue Retriever 6MM x 25MM |
| Affected: | |
| Software version: | |
| Recalling Organisation: | Stryker New Zealand Ltd 515 Mount Wellington Highway Mount Wellington AUCKLAND 1060 |
| Contact Information: | 0800 787 9287 |
| Manufacturer: | Stryker Neurovascular |
| Issue: | The manufacturer has observed an increase in global complaints involving fractures of the core wires of the Trevo® XP ProVue Retriever for certain lots manufactured between the time period of 22-JUL-2019 to 09-SEP-2019 resulting in stent retriever separation from the core wire during use. |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 2/10/2020 |
