Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 31429 |
| Brand Name: | Angiographic X-Ray |
| Model: | Model numbers - 459800772231, 459800772233, 459800772261, 459800772263, 459800415531, 459800415532, 459800415533 ,459800415534, 459800415535, 459800415571, 459800415572, 459800415573, 459800415574, 459800415575 |
| 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 become aware of several situations that can result in a loss of availability of the wireless foot switch during a procedure. Identified issues that may result in the wireless foot switch not being available are: · Loss of Bluetooth connection due to interferences from other radio equipment · Battery not fully charged · Battery not holding its charge · Damage in the charger, cable and/or connector of the wireless foot switch |
| Recall action type: | Correction |
| Recall action: | Product to be modified |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 3/7/2023 |
