Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 15353 |
| Brand Name: | Philips BrightView XCT Imaging System |
| Model: | Product Code: 882482 & 882454 |
| Affected: | All 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 Radiation Oncology Systems |
| Issue: | Philips received a report from the field that the FPD failed to remain securely latched in the stowed position. A system WARNING message appeared warning the user that the FPD was unlatched. By design, the unlatching of the FPD caused the system to activate the e-stop. In an attempt by the operator to clear the warning message while in the 0 degree position, the FPD released from the stowed position. |
| Recall action type: | Correction |
| Recall action: | Product to be modified |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 16/9/2013 |
