Toshiba American Med Sys Inc Magnetic Resonance Imaging, System: Flexart, Visart and Excelart Models. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Magnetic Resonance Imaging, System: Flexart, Visart and Excelart Models.
Brand
Toshiba American Med Sys Inc
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
Flexart systems with software V3.51*R534 to V4.10*R551. Visart systems with software V3.51*R234 to V4.10*R251. Excelart systems with softare V4.04*R251 to V4.10*R271.
Toshiba American Med Sys Inc is recalling Magnetic Resonance Imaging, System: Flexart, Visart and Excelart Models. due to Software anomally causes image slices to be in incorrect order.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Software anomally causes image slices to be in incorrect order.
Recommended Action
Per FDA guidance
Firm sent letters to customers 1/28/2004 which explains how to avoid the adverse event and announces that a software fix is going to be made available.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA, CO, FL, NV, NJ, NY, OH, OK, OR, PA, TN, TX, PR
Page updated: Jan 10, 2026