Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 14676 |
| Brand Name: | Philips MammoDiagnost DR Digital mammography system |
| Model: | |
| Affected: | Software release 2.1 |
| 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 DMC GmbH |
| Issue: | The dose exceeds levels set by local regulations in Sweden, New Zealand and Australia when Automatic Exposure Control (AEC) is used and the exposure time in magnification mode is too long. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 17/5/2013 |
