Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 19511 |
| Brand Name: | Philips Ingenuity CT/Core/Core128, Brilliance 64 CT/iCT SP/iCT |
| Model: | Ingenuity CT/Core/Core128, Brilliance 64 CT/iCT SP/iCT |
| Affected: | Software versions: 4.1.2, 4.1.3, 4.1.4 |
| Software version: | |
| Recalling Organisation: | Philips New Zealand Commercial Limited Level 3 123 Carlton Gore Road Newmarket AUCKLAND 1023 |
| Contact Information: | 0800 251 400 |
| Manufacturer: | Philips Medical Systems |
| Issue: | On the affected CT systems and software versions, the perfusion scan feature may be unavailable. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 2/12/2015 |
