Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 36702 |
| Brand Name: | Corpuls 3 Defib including Accessories and Upgrades |
| Model: | Corpuls 3 / Corpuls 3 Touch |
| Affected: | Software versions SW-REL-4.3.3, 4.4.2, or 4.4.3 |
| 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: | In corpuls3 modules running software versions SW-REL-4.3.3, 4.4.2, or 4.4.3 in combination with a license for automatic ECG interpretation (Glasgow Full Scale or HES), an internal configuration file may, in very rare cases, be lost during the boot process. This behaviour occurs randomly and cannot be influenced by the user. If this condition occurs, the functions for automatic ECG interpretation and the specific ECG alarms (corpuls ACS) are not available. The basic device functions for ECG signal acquisition and display remain available. The alarm message Possible acute STEMI also remains available and is therefore not affected. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 30/3/2026 |
