Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 19056 |
| Brand Name: | Covidien Medi-Trace Cadence Adult Multi-Function Defibrillator electrode |
| Model: | 22550PC & 22770PC |
| Affected: | 517521X, 519835X & 516313X, 519124X, 513426X |
| Software version: | |
| Recalling Organisation: | Covidien NZ Ltd Level 3, Building 5, Central Park Corporate Centre 666 Great South Road Penrose AUCKLAND 1051 |
| Contact Information: | 0508 489 264 |
| Manufacturer: | Covidien LLC |
| Issue: | The manufacturer advises there is a low-level potential for damage to the wire insulation. The use of products with this condition may result in a potentially increased risk for reduced or no patient therapy, arcing of current, sparking, and patient and/or clinician burns. |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 28/8/2015 |
