Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 23573 |
| Brand Name: | Thermablate |
| Model: | Treatment Control Unit - product code 22101 and Thermablate Disposable Cartridge - product code 21004-S. |
| Affected: | |
| Software version: | |
| Recalling Organisation: | New Zealand Medical & Scientific Ltd Level 4, Building 10 666 Great South Road Ellerslie AUCKLAND 1051 |
| Contact Information: | 09 259 4062 |
| Manufacturer: | Idoman Teoranta |
| Issue: | The manufacturer is informing costomers that there has been an update to the informantion for Use (IFU) document for the Thermablate EAS System which comprises of the Treatment Control Unit and the Thermablate Disposable Cartridge. |
| Recall action type: | Correction |
| Recall action: | Instructions for use to be updated |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 10/9/2018 |
