Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 13882 |
| Brand Name: | Philips Brilliance CT Big Bore CT scanners with TumorLOC software |
| Model: | |
| Affected: | TumourLOC version prior to 3.6 |
| 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 |
| Brand Name: | Philips Gemini LXL, Gemini TF16, Gemini TF64, and Gemini TF Big Bore PET/CT Combination with TumorLOC software |
| 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 |
| Brand Name: | Philips Extended Brilliance Workstation (EBW) with TumorLOC software |
| 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 Radiation Oncology Systems |
| Issue: | The TumorLOC application has the capability to generate intensity projection datasets from respiratory gated data. The manufacturer has identified a circumstance where these generated datasets are flipped and incorrectly labeled left to right when they are saved to disk. |
| Recall action type: | Correction |
| Recall action: | Instructions for use to be updated |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 4/12/2012 |
