Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 36821 |
| Brand Name: | Philips Azurion Systems Angiographic X-Ray |
| Model: | Philips Azurion 7 M20 Systems - system code 722079 |
| 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 |
| Issue: | The manufacturer has identified that the Float Tabletop control on the control module of Azurion systems may experience mechanical wear over time. The Float Tabletop control is located on the control module at the table-side. When the control is actuated, the table brakes disengage, allowing adjustment of the longitudinal or transverse position of the table. Over time, mechanical wear may lead to detachment, cracking, or breakage of the Float Tabletop control, which may lead to reduced availability or unavailability of longitudinal and transverse tabletop movement, as well as the formation of sharp edges. |
| Recall action type: | Correction |
| Recall action: | Product to be modified |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 19/5/2026 |
