Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 21189 |
| Brand Name: | Cordis SMART Flex Vascular Stent System |
| Model: | |
| Affected: | Lot range 34469 through 39974 |
| Software version: | |
| Recalling Organisation: | InterMed Medical Ltd 71 Apollo Drive Albany AUCKLAND 1311 |
| Contact Information: | 0800 333 444 |
| Manufacturer: | Cordis Corporation |
| Issue: | Based on complaints and subsequent investigation, the manufacturer has determined that SMART Flex Vascular Stents System size 5x200mm and 6x200mm have been associated with an higher frequency of incidents of deployment difficulty. |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 10/3/2017 |
