Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 15039 |
| Brand Name: | Philips Brilliance iCT and iCT SP |
| Model: | |
| Affected: | |
| Software version: | up to an inc,uding version 3.2.5 |
| 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: | When using 80 kVp with intravenous contrast in head and neck studies with U-filters (UA, UB, UC) a vascular artifact that resembles thrombus may appear on the image. There is a risk of misdiagnosis which can lead to unnecessary treatment of a patient. |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 25/7/2013 |
