Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 16604 |
| Brand Name: | Philips Brilliance CT series and Ingenuity CT series systems |
| Model: | Brilliance CT 16, 64, Big Bore, iCT, Ingenuity CT, Ingenuity Core, Ingenuity Core128, Ingenuity Flex |
| Affected: | |
| 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 has determined there are two potential issues that may result in the subframe of the table top becoming free floating and causing unintended, horizontal motion. The two potential issues are: 1. Service latch may not be properly secured 2. Service latch threaded rod may be fractured To date, there have been no reported injuries or deaths resulting from these issues. |
| Recall action type: | Correction |
| Recall action: | Product to be modified |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 1/5/2014 |
