PlainRecalls
FDA Devices Moderate Class II Ongoing

MRI system: Vantage Elan, Model: MRT-2020

Reported: March 13, 2024 Initiated: January 29, 2024 #Z-1249-2024

Product Description

MRI system: Vantage Elan, Model: MRT-2020

Reason for Recall

For some MRI systems, it has been found that some of the maximum Spatial Field Gradient (SFG) values displayed in "System Information" of the operation window and some of the maximum SFG values described in the safety manual are lower than the correct values, which may cause a patient with an MR conditional device to feel some discomfort during the MR scan.

Details

Units Affected
1
Distribution
Worldwide - US Nationwide distribution including in the states of MD, IL, WV, CA, AZ, PR, CO, GA, PA, WA, UT, OK, KY, IA, IN, TN, CT, WI, OH, AL, MT, NM, TX, MO, MN, OR, ID, WY, NV, AR, FL, SD, MI, NY, NJ, KS, LA, NH, VT, MS, SC, ME and the country of DO.
Location
Tustin, CA

Frequently Asked Questions

What product was recalled?
MRI system: Vantage Elan, Model: MRT-2020. Recalled by Canon Medical System, USA, INC.. Units affected: 1.
Why was this product recalled?
For some MRI systems, it has been found that some of the maximum Spatial Field Gradient (SFG) values displayed in "System Information" of the operation window and some of the maximum SFG values described in the safety manual are lower than the correct values, which may cause a patient with an MR conditional device to feel some discomfort during the MR scan.
Which agency issued this recall?
This recall was issued by the FDA Devices on March 13, 2024. Severity: Moderate. Recall number: Z-1249-2024.