Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 25764 |
| Brand Name: | Corpuls 3 Defib including Accessories and Upgrades |
| Model: | CORPULS 3 Software versions 3.1.0, 3.1.1, and 3.1.2 |
| Affected: | |
| Software version: | |
| Recalling Organisation: | Universal Specialities Ltd trading as USL Medical 494 Rosebank Road Avondale AUCKLAND 1026 |
| Contact Information: | 09 829 0595 |
| Manufacturer: | GS Elektromedizinische GmbH |
| Issue: | When using the therapy functions (Manual and AED) the curve of the ECG lead DEauto may switch unexpectedly to lead IIauto, showing a faulty ECG signal (= malfunction), (see error description). As a safety measure the manufacturer has decided to update all corpuls3 devices that are operating with the affected software version with a new software version. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 4/3/2020 |
