Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 20148 |
| Brand Name: | Cordis PRECISE PRO Rx Nitinol Stent System |
| Model: | Multiple lot numbers |
| Affected: | Product manufactured between April 27, 2015 and November 22, 2015. |
| Software version: | |
| Recalling Organisation: | Johnson & Johnson (New Zealand) Limited 507 Mt Wellington Highway Mt Wellington AUCKLAND 1060 |
| Contact Information: | 0800 922 638 |
| Manufacturer: | Cordis Corporation |
| Issue: | Based on complaints and subsequent investigation, the manufacturer has detected an increased frequency of users reporting difficulty with stent deployment and/or separation of the bond between sections of the device outer member. The manufacturer has isolated the issue to product manufactured between April 27, 2015 and November 22, 2015. Product that has been manufactured after November 22, 2015, is not affected. |
| Recall action type: | Recall |
| Recall action: | Product to be destroyed |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 11/5/2016 |
