Recall Z-0163-2026

IMPRIS Imaging Inc · initiated September 30, 2025

Class I Open, Classified

Class I – dangerous or defective products that could cause serious health problems or death

Product

IMRIS Operating Suite, IMRIS iMRI 3T V, containing Siemens 3 Tesla MRI Magnet, vIDA

Codes / lots: IMRIS Part Number(s): 120823-000, UDI/DI 00857534006745

Reason for recall

There is a potential safety issue associated with the magnet venting paths of the Siemens 3 Tesla MRI system within your IMRIS Operating Suite. Siemens notified IMRIS that an ice blockage may exist within the magnet venting system. In the event of a quench, helium gas may be unable to escape through the designed vent paths, leading to a pressure build-up within the helium containment system which could ultimately rupture the helium containment system, potentially resulting in a helium leak into the scanning room.

FDA-determined cause: Under Investigation by firm

Action taken

Imris issued an URGENT: MEDICAL DEVICE CORRECTION notice to its consignees on 9/30/2025 via email. The notice explained the issue, the risk to health, and provided the following information: "If the error message, "Magnet Supervision: The average heater power is above the alarm threshold. Please contact Siemens Service." appears, DO NOT REBOOT THE SYSTEM. Please call your local Siemens Healthineers service organization. Grant access to the system so that the inspection can be carried out as directed by Siemens Healthineers service organization." "Please immediately instruct your personnel accordingly, and please contact our customer support team via our service line at 1-866-475-0525 or e-mail at customersupport@imris.com if you have any questions or concerns. Please keep this information until the corrective measures have been finalized." This notice included a copy of the Siemens Healthineers Urgent Medical Device Correction notice.

Details

Recall number
Z-0163-2026
Initiated
September 30, 2025
Posted by FDA
October 28, 2025
Product code
LNH – System, Nuclear Magnetic Resonance Imaging
Distribution
Worldwide distribution - US Nationwide and the countries of Canada, Sweden, Switzerland, Japan, Australia, Qatar, and China.
Recalling firm
IMPRIS Imaging Inc, Chaska, MN

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-0161-2026 Class IIMRIS Operating Suite, Neuro III-SV iMRI System, iMRX System, containing Siemens 3 Tesla…There is a potential safety issue associated with the magnet venting paths of the Siemens 3 Tesla MRI system… 09/30/2025Open, Classified
Z-0162-2026 Class IIMRIS Operating Suite, iMRI 3T S, containing Siemens 3 Tesla MRI Magnet, SkyraThere is a potential safety issue associated with the magnet venting paths of the Siemens 3 Tesla MRI system… 09/30/2025Open, Classified
Z-0164-2026 Class IIMRIS Operating Suite, InVision 3T Operating Suite, containing Siemens 3 Tesla MRI…There is a potential safety issue associated with the magnet venting paths of the Siemens 3 Tesla MRI system… 09/30/2025Open, Classified