# FDA recall Z-3023-2018

> **NordicNeuroLab AS** · Class II · device recall initiated 2018-08-20.

## Product

fMRI Hardware System   VisualSystem allows video signals from the stimulus presentation PC to enter the shielded scanner room and presented by a set of coil-mounted displays or by an in-room LCD monitor.  - LCD Monitor Power supply (LPS) for LCD Monitor, Versions 1.0 and 1.1

## Reason for recall

Complaints of this version of the power supply unit (LPS) (1.0 and 1.1) being dragged into the magnet bore (MR Scanner).

## Distribution

worldwide

## Key facts

- **Recall number:** Z-3023-2018
- **Recalling firm:** NordicNeuroLab AS
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-08-20
- **Report date:** 2018-09-19
- **Termination date:** 2020-09-16

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Bergen, N/A, Norway

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3023-2018

## Citation

> AI Analytics. FDA recall Z-3023-2018. Retrieved 2026-07-08 from https://api.ai-analytics.org/recall/Z-3023-2018. Source: US FDA. Licensed CC0.

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