Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 20280 |
| Brand Name: | Philips BrightView SPECT/CT Combination |
| Model: | BrightView XCT |
| 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 Radiation Oncology Systems |
| Issue: | During a non-Auto Body Contouring (ABC), non-circular, rel-180 scan, the detector may come in contact with the patient. If this occurs, contact sensors would pause the scan. The manufacturer has released a revised letter( 26/08/2016) which includes further detail specific to software version to the problem description, how to identify affected products, and advice on actions for customer clarity. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 16/6/2016 |
