Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 26687 |
| Brand Name: | Efficia DFM100, HeartStart Intrepid |
| Model: | All Philips Efficia Defibrillator/Monitor (Model number 866199) manufactured prior to March-30th-2020 |
| 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 Goldway (Shenzhen) Industrial Inc |
| Issue: | The manufacturer has determined that the 866199 Efficia DFM100 Defibrillator/Monitor may give a false low battery indication, caused by a voltage inrush, when the battery is inserted or removed. |
| Recall action type: | Correction |
| Recall action: | Product to be modified |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 12/10/2020 |
