Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 17985 |
| Brand Name: | Philips Brilliance and Ingenuity CT Systems |
| Model: | Brilliance CT 16 Air, 64, Big Bore, iCT, iCT SP, Ingenuity CT, Ingenuity Core, Ingenuity Core128 and Ingenuity Flex |
| Affected: | Specific lot 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: | A potential problem with the vertical motor / brake assembly on the patient support / couch was discovered with a specific patient support / couch manufacturing lot, which may result in uncommanded vertical patient support / couch motion. To date, there have been no reported occurrences of harm. |
| Recall action type: | Correction |
| Recall action: | Product to be modified |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 20/1/2015 |
