Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 25152 |
| Brand Name: | Brightview, Brightview X |
| Model: | 882020 Forte, 882320 Forte JETStream AZ |
| 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 manufacturer has identified an issue affecting the Forte family of gamma cameras that could result in either detector 1 or detector 2 falling unimpeded vertically to the end stops of its travel limit, due to a mechanical failure, possibly making contact with a patient that could result in entrapment, serious injury, or death. |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 30/9/2019 |
