Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 16603 |
| Brand Name: | Philips Brilliance CT, Ingenuity CT, Ingenuity Core, Ingenuity Core 128, Ingenuity Flex, MX8000 Dual |
| Model: | |
| 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 have found if the service latch is not properly secured during servicing of the device, the table top's subframe becomes free floating causing unintended, horizontal motion. To date, there have been no reported injuries or deaths resulting from this issue. |
| Recall action type: | Correction |
| Recall action: | Product to be modified |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 30/4/2014 |
