Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 27351 |
| Brand Name: | Cordis_PRECISE PRO Rx Stent |
| Model: | |
| Affected: | Multiple lot numbers |
| Software version: | |
| Recalling Organisation: | InterMed Medical Ltd 71 Apollo Drive Albany AUCKLAND 1311 |
| Contact Information: | 0800 333 444 |
| Manufacturer: | Cordis Corporation |
| Issue: | The manufacturer has receive reports for distal tip separation from the wire lumen that may be the result of inadequate joint adhesion. They have isolated the issue to particular lots of product made between October 2019 and August 2020. |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Wholesale |
| Date Commenced: | 26/2/2021 |
