Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 20820 |
| Brand Name: | Brilliance iCT Ingenuity CT |
| Model: | |
| Affected: | Brilliance iCT / Brilliance iCT SP, Brilliance Big Bore Oncology / Brilliance Big Bore Radiology, Brilliance 6 / Brilliance 10 / Brilliance16/ Brilliance 16P / Brilliance 40 / Brilliance 64,Ingenuity CT / Ingenuity Core / Ingenuity Core128 |
| 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: | The patient support table top may fail to move in the horizontal direction when it is commanded to do so during CT scans, due to a potential mechanical linkage failure. The system cannot automatically detect this failure to abort the scan or to alert the user. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 9/11/2016 |
