Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 22217 |
| Brand Name: | ELUVIA™ Drug-Eluting Vascular Stent System |
| Model: | |
| Affected: | Innova 200mm - EU |
| Software version: | |
| Recalling Organisation: | Boston Scientific NZ Ltd 3 Diamond Street Eden Terrace Auckland 1021 |
| Contact Information: | 0800 742 678 |
| Manufacturer: | Boston Scientific Corporation |
| Brand Name: | Prosthesis, Internal, Stent, Vascular |
| Model: | |
| Affected: | Eluvia 150mm- OUS |
| Software version: | |
| Recalling Organisation: | Boston Scientific NZ Ltd 3 Diamond Street Eden Terrace Auckland 1021 |
| Contact Information: | 0800 742 678 |
| Manufacturer: | Boston Scientific Corporation |
| Issue: | Partial deployment occurs when the stent is unable to be fully released from the delivery system. Part of the stent can become anchored in the vessel while the rest of the stent remains within the delivery system. |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 6/11/2017 |
