Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 27603 |
| Brand Name: | Veniti_58057_IIbVici Venous Stent System |
| Model: | |
| Affected: | Multiple lots |
| Software version: | |
| Recalling Organisation: | Clinical & Regulatory Services Limited 30 Fulford Road Havelock North Hastings 4130 |
| Contact Information: | (06) 844 4490 |
| Manufacturer: | Veniti, Inc |
| Issue: | The manufacturer has received reports of stent migration after implantation. Some stent migrations have led to the need for endovascular intervention to secure or retrieve the stent. In more severe cases, the stent has embolized to the heart, resulting in the need for surgery. |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 16/4/2021 |
