Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 24207 |
| Brand Name: | Cordis_Tip Guiding Catheter |
| Model: | |
| Affected: | Catalogue number - CO-67005400 and CO-67205400 |
| Software version: | |
| Recalling Organisation: | InterMed Medical Ltd 71 Apollo Drive Albany AUCKLAND 1311 |
| Contact Information: | 0800 333 444 |
| Manufacturer: | Cordis Corporation |
| Issue: | Frayed pieces of the mounting card were found in the sterile primary package. While the material may be identified when the product is opened and prepared for use, there is a potential for harm if the material is not discovered or if the device is not prepared properly |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 21/2/2019 |
