Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-3023-2018 — 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

U.S. FDA — Device Enforcement · Norway · 2018-08-20 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-3023-2018
Date of alert
2018-08-20
Country / jurisdiction
Norway
Risk level
Class II
Risk type
recall
Brand
NordicNeuroLab AS
Product category
device
Product type
Devices
Reported risk: Complaints of this version of the power supply unit (LPS) (1.0 and 1.1) being dragged into the magnet bore (MR Scanner).
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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