Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 31716 |
| Brand Name: | Azurion MDR |
| Model: | wired and wireless foot switch - Allura Xper, Allura Centron, Azurion and MultiDiagnost-Eleva systems. Multiple serial numbers |
| 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 Nederland BV |
| Brand Name: | MultiDiagnost-Eleva systems |
| Model: | wired and wireless foot switch - Allura Xper, Allura Centron, Azurion and MultiDiagnost-Eleva systems. Multiple serial numbers |
| 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 Nederland BV |
| Brand Name: | Angiographic X-Ray |
| Model: | wired and wireless foot switch - Allura Xper, Allura Centron, Azurion and MultiDiagnost-Eleva systems. Multiple serial numbers |
| 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 Nederland BV |
| Brand Name: | Allura Centron |
| Model: | wired and wireless foot switch - Allura Xper, Allura Centron, Azurion and MultiDiagnost-Eleva systems. Multiple serial numbers |
| 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 India Ltd |
| Issue: | The manufacturer has updated the Product Correction letter dated 7-Aug-2023 (ref. 2023-IGT-BST-013) related to the Potential of the wired and wireless foot switch to become stuck in the active position resulting in unintended radiation of the Philips Allura Xper, Allura Centron, Azurion and MultiDiagnost-Eleva systems. The updates were to include: A link/QR code for a video demonstration of the cleaning process and the use of the protective bag. A reminder to report to Philips any event related to a foot switch getting stuck resulting in unintended radiation of any amount. Updates to the Instructions for Use (IFU) addendum to include instructions related to additional foot switch in the examination room and a recommended placement of the additional footswitch. |
| Recall action type: | Correction |
| Recall action: | Instructions for use to be updated |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 21/11/2023 |
