Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 28633 |
| Brand Name: | CombiDiagnost R90 |
| Model: | Model number - 709030, 709031 |
| 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 DMC GmbH |
| Brand Name: | CombiDiagnost R90 (MDR) |
| Model: | Model number - 709130 |
| 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 DMC GmbH |
| Issue: | If the CombiDiagnost R90 system experiences a short circuit of the Electromagnetic Interference (EMI) filter or UA/UB board, there is a potential for the user to see/smell smoke and/or hear a popping sound coming from the Main-cabinet (M-cabinet). This can occur at any time if a wire is damaged and connected to the ground or the system experiences a power surge. There is a potential risk of smoke inhalation to patients, operators, or bystanders. |
| Recall action type: | Correction |
| Recall action: | Product to be modified |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 22/11/2021 |
