NordicNeuroLab recalls fMRI hardware power supplies (LPS 1.0/1.1) that may drag into MRI scanner, causing injury. Affected units have specific serial numbers.
Complaints of this version of the power supply unit (LPS) (1.0 and 1.1) being dragged into the magnet bore (MR Scanner).
NordicNeuroLab is recalling fMRI hardware power supplies that could be pulled into the MRI scanner, potentially causing injury. This affects specific versions with serial numbers starting with LPS-2011-1.0-XXX or similar.
The power supply units (LPS) versions 1.0 and 1.1 can be dragged into the MRI scanner's magnet bore during operation. This risk occurs when the power supply moves toward the scanner, potentially causing injury to users or damaging the equipment.
Users of NordicNeuroLab's fMRI VisualSystem hardware with specific power supply versions (LPS 1.0 and 1.1) are affected. MRI facility staff and researchers using these systems are most at risk.
Check for power supply units with serial numbers starting with LPS-2011-1.0-XXX, LPS-2012-1.0-XXX, LPS-2012-1.1-XXX, or LPS-2013-1.1-XXX. These are versions 1.0 and 1.1 of the LPS for the fMRI VisualSystem.
Look for serial numbers starting with LPS-2011-1.0-XXX, LPS-2012-1.0-XXX, LPS-2012-1.1-XXX, or LPS-2013-1.1-XXX on the power supply unit.
The power supply units (LPS) versions 1.0 and 1.1 can be dragged into the MRI scanner's magnet bore, potentially causing injury.
Check the serial number on the power supply; affected units start with LPS-2011-1.0-XXX, LPS-2012-1.0-XXX, LPS-2012-1.1-XXX, or LPS-2013-1.1-XXX.
The recall does not specify a remedy, so no action is required beyond checking if your power supply has the affected serial numbers.
We’ve drafted a message you can send NordicNeuroLab to request your refund or repair — edit it as you like.
Subject: Recall Z-3023-2018 — NordicNeuroLab NordicNeuroLab Hello, I own a NordicNeuroLab that is covered by recall Z-3023-2018 from NordicNeuroLab. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
