Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 14740 |
| Brand Name: | Philips Precedence SPECT/CT System utilising Brilliance CT |
| Model: | Product Code(s): 882350, 882351 |
| 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 |
| Brand Name: | Philips Brilliance CT Systems |
| Model: | Product Code(s): 728256, 728251, 728246, 728240, 728235, 728231, 728243, 728244, 728306, 728311 |
| 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 Gemini PET/CT Combination utilising Brilliance CT |
| Model: | Product Code(s): 882160, 882300, 882390, 882400, 882410, 882412, 882470, 882473, 882471, 882476 |
| 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: | The stated tolerance for CTDIvol in the Instructions for Use Manual did not accurately represent all systems. On some systems the measured CTDIvol value may fall outside of these stated tolerances |
| Recall action type: | Correction |
| Recall action: | Instructions for use to be updated |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 30/5/2013 |
