FDA recall record

Canon Medical System, USA MRI systems: Vantage Orian MRT-1550 (MEXL-1550), Vantage Elan recall — FDA Z-2041-2024

The terminal block used to secure the power supply cable for the gradient coil of the MRI system was not secured as designed, which could cause cable…

Class IIclassification
Z-2041-2024official record ID
Jun 19, 2024report date

Recall record at a glance

Official recordZ-2041-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmCanon Medical System, USA, Inc.
Report dateJun 19, 2024
Recall initiation dateMay 10, 2024
Quantity153
LocationTustin, CA, United States

Official product description

MRI systems: Vantage Orian MRT-1550 (MEXL-1550), Vantage Elan MRT-2020 (MEXL-1520), Vantage Titan MRT-1504 (MEXL-1504), Vantage Titan 3T MRT-3010 (MEXL-3010), Vantage Galan 3T MRT-3020 (MEXL-3020)

Why the product was recalled

The terminal block used to secure the power supply cable for the gradient coil of the MRI system was not secured as designed, which could cause cable disconnection, which could lead to arcing, followed by melting of the cable, ignition, smoke, and fire.

Distribution information

US: PA, SC, IA, AL, MI, AR, SD, TX, ID, KY, NY, MN, MD, OH, WI, NV, CT, AZ, IL, OK, CA, FL, GA, OR, IN, NJ, CO, MT, KS, MO, WY, VA, VT, LA, NH, WV, TN, PR

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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About this record

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