Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 37529 |
| Brand Name: | [MDR] Spectral CT, IQon Spectral CT, Brilliance iCT, Brilliannce iCT Upgrade |
| Model: | Product code: 738333 Spectral CT |
| Affected: | Software version - V5.0.x, V5.2.x, V5.4.x |
| 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 Nederland BV |
| Brand Name: | BEST CT Systems |
| Model: | Product code: 738333 Spectral CT |
| Affected: | Software version - V5.0.x, V5.2.x, V5.4.x |
| 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 Nederland BV |
| Issue: | The manufacturer has identified 24 software issues that may affect certain Spectral CT systems. Affected customers will be contacted to arrange installation of the necessary software update to resolve these issues. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 14/9/2026 |
