Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 25510 |
| Brand Name: | Tempus LS |
| Model: | |
| Affected: | All Tempus LS on the market within listed s/n range are affected; Serial Numbers: 7021.000100 up to 7021.001215 |
| Software version: | |
| Recalling Organisation: | Philips New Zealand Commercial Limited Level 3 123 Carlton Gore Road Newmarket AUCKLAND 1023 |
| Contact Information: | 0800 251 400 |
| Manufacturer: | Schiller AG |
| Issue: | The manufacturer has identified that under certain circumstances a defibrillation will not be possible. It's possible that an impedance change between patient and device causes an impairment of the impedance measurement. If the impedance is out of a valid range, a defibrillation is not possible. Issue 2: Unexpected safety discharge The manufacturer received notice that under certain circumstances the device performs an unexpected safety discharge. |
| Recall action type: | Correction |
| Recall action: | Product to be modified |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 7/1/2020 |
