Toshiba American Med Sys Inc Magnetic Resonance Imaging Systems under the following names: Visart Excelart Excelart P2 Excelart P3 Excelart SPIN Excelart VANTAGE 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 Excelart VANTAGE
Brand
Toshiba American Med Sys Inc
Lot Codes / Batch Numbers
All serial numbers.
Products Sold
All serial numbers.
Toshiba American Med Sys Inc is recalling Magnetic Resonance Imaging Systems under the following names: Visart Excelart Excelart P2 Exce due to Software defect causes images to be rotated 180 degrees.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Software defect causes images to be rotated 180 degrees.
Recommended Action
Per FDA guidance
Firm sent a letter to consignees October 6, 2004 describing the observed conditions causing the flaw to manifest itself. A workaround solution is also described in the letter. A software correction is under development and will be installed by a TAMS representative in the future.
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