Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 37492 |
| Brand Name: | Philips CT Areta/Rembra systems |
| Model: | CT Rembra RT |
| Affected: | CT Areta/Rembra software version 6.0.0.X |
| 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 Healthcare (Suzhou) Co Ltd |
| Issue: | The manufacturer has identified multiple software issues in CT Areta/Rembra software version 6.0.0.X. These issues may result in reconstruction failures, scan interruptions, image artifacts, positioning inaccuracies, or corrupted images. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 7/9/2026 |
