Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
IMRIS IMRI 1.5T AND 3T S System Product Usage: The Recalled by Deerfield Imaging, Inc. Due to The DC power to the IFOSS collision detector...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Deerfield Imaging, Inc. directly.
Affected Products
IMRIS IMRI 1.5T AND 3T S System Product Usage: The IMRIS intraoperative MRI systems are traditional MRI systems that have been suspended on an overhead rail system. and is designated to operative inside an RF shielded room to facilitate intraoperative and multi room use.
Quantity: 10 units
Why Was This Recalled?
The DC power to the IFOSS collision detector control panel at your facility is being adversely affected by the magnetic field. Our investigation shows the magnetic field is causing the IFOSS control panel to malfunction.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Deerfield Imaging, Inc.
Deerfield Imaging, Inc. has 19 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report