Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 14079 |
| Brand Name: | Philips Brilliance CT series |
| Model: | Models: 6, 10, 16, Power 40, 64, CT Big Borte, CT Big Bore Oncology, iCT, iCT SP, Ingenuity Core, Ingenuity CT and MX8000 Dual v.EXP |
| Affected: | Selected serial numbers |
| 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: | Philips Healthcare received reports from the field stating the patient table on a system had an unexpected downward movement while a patient was on the table. |
| Recall action type: | Correction |
| Recall action: | Product to be modified |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 14/1/2013 |
