Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 24252 |
| Brand Name: | Angiographic X-Ray |
| Model: | |
| Affected: | Allura Xper FD20 - Bent Pedals of Footswitch |
| 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 if a Footswitch is frequently used on an anti-fatigue mat, on a non-flat surface or in the pedestal, the footswitch pedals may get bent, which might lead to an intermittent or continuous inability of making live fluoroscopy images or exposures. |
| Recall action type: | Correction |
| Recall action: | Product to be modified |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 4/3/2019 |
