Toshiba American Med Sys Inc Magnetic Resonance Imaging Systems, under the following names: Visart Excelart Excelart P2 Excelart P3 Excelart SPIN Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Magnetic Resonance Imaging Systems, under the following names: Visart Excelart Excelart P2 Excelart P3 Excelart SPIN
Brand
Toshiba American Med Sys Inc
Lot Codes / Batch Numbers
No specific codes were listed.
Products Sold
No specific codes were listed.
Toshiba American Med Sys Inc is recalling Magnetic Resonance Imaging Systems, under the following names: Visart Excelart Excelart P2 Excel due to Software defect causes patient identification number to be truncated.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Software defect causes patient identification number to be truncated.
Recommended Action
Per FDA guidance
Firm issued a letter notifying users of systems that when transferring image data to a DICOM server for any patient born on January 1, to verify that the Patient ID is correct on the DICOM server after the transfer. Firm will modify the software by January 2005.
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 noticePage updated: Jan 10, 2026