Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 22314 |
| Brand Name: | CombiDiagnost R90 |
| Model: | |
| Affected: | All CombiDiagnost |
| 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 manufacturer has become aware that in some CombiDiagnost deliveries the tube adapter-plate green/yellow protective earthing wire was removed During GCF tubes assembly, spacers with different thickness are used to position pre-loc ring in respect to focal spot in specified distance. There is a potential of an electrical shock if following factors occurs: 1. An electrical failure leads to an electrical potential on the adapter plate 2. The earth resistance based on mechanical connection is beyond limit 3. Person removes the tube cover. (not allowed for the customer) 4. Person touches the live wired part during exposure/fluoroscopy. |
| Recall action type: | Correction |
| Recall action: | Product to be modified |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 24/11/2017 |
