[Recalled] NBS System 4 (sw version 4.0 or higher), Software update to 4.3.3 and NBS System 5 (sw version 5.0 or higher), Software update to 5.1.1. The Nexstim Navigated Brain Stimulation System (NBS System) is indicated for noninvasive ma
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | NBS System 4 (sw version 4.0 or higher), Software update to 4.3.3 and NBS System 5 (sw version 5.0 or higher), Software update to 5.1.1. The Nexstim Navigated Brain Stimulation System (NBS System) is indicated for noninvasive mapping of the primary motor cortex of the brain to its cortical gyrus. T |
|---|---|
| Brand / manufacturer | Nexstim PLC |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2320-2017 |
| Country of notice | Finland |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 14 March 2017 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Software defect: the NBS software may accidentally generate duplicate copies of one or several files.
This Class II recall concerns device products distributed in Finland 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 Nexstim PLC
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.