Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 29116 |
| Brand Name: | CORE Systems, IntraSight System |
| Model: | |
| Affected: | commercial part number 797403, Part numbers: 300002018101, 30000201810 |
| Software version: | |
| Recalling Organisation: | Philips New Zealand Commercial Limited Level 3 123 Carlton Gore Road Newmarket AUCKLAND 1023 |
| Contact Information: | 0800 251 400 |
| Manufacturer: | Volcano Corporation |
| Issue: | The manufacturer has identified a potential issue with the Philips Multi-Modality Touch Screen Module (MM-TSM) bedside/secondary control unit for the IntraSight system. The MM-TSM is susceptible to cracking, which may impact usability of the bedside/secondary controller depending on location and severity of touch screen damage. |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 14/3/2022 |
