[Recalled] EPWorks software used in the Protektor 32 Product Usage: Uses electroencephalography (EEG), evoked potentials (EP), electromyography (EMG) and transcranial motor evoked potentials (TcMEP) stimulation techniques to provide hea
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | EPWorks software used in the Protektor 32 Product Usage: Uses electroencephalography (EEG), evoked potentials (EP), electromyography (EMG) and transcranial motor evoked potentials (TcMEP) stimulation techniques to provide healthcare professionals with information to help assess patients neurolo |
|---|---|
| Brand / manufacturer | Natus Medical Incorporated |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1067-2015 |
| Country of notice | Canada |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 02 January 2015 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Software error occurs when using remote monitoring; if the remote user tries to stop the free run waveform group, the system will display a message informing the user that they do not have sufficient privilege.
This Class II recall concerns device products distributed in Canada and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Natus Medical Incorporated
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.