Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 29229 |
| Brand Name: | General Ultrasound Imaging System |
| Model: | Philips EPIQ and Affiniti Ultrasound Systems |
| 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 Ultrasound LLC |
| Issue: | The manufacturer has identified software issues associated with the Auto Measure feature. These issues may lead to the display of incorrect values in the Auto Measure results box, final report, or both, potentially leading to the need for re-measurement of values. These issues are specific to user workflows associated with the manual edit or manual trace option. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 7/4/2022 |
