Toshiba American Med Sys Inc Toshiba Excelart VANTAGE Model MRT-1503, Magnetic Resonance Imaging Systems, Regulation Number 21 CPR 892.1000, Regulatory Class II, Product Code 90-LNH and was cleared with K032490 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Toshiba Excelart VANTAGE Model MRT-1503, Magnetic Resonance Imaging Systems, Regulation Number 21 CPR 892.1000, Regulatory Class II, Product Code 90-LNH and was cleared with K032490
Brand
Toshiba American Med Sys Inc
Lot Codes / Batch Numbers
Serial Numbers: A4622037, A4612031, A4622017, A4532013, A4582010, A5532048, A4592013, A4532012, A5532022, A4602028, A3592003, A4522007, A5512041, A4612015, A4572020, A4602029, A4622039, A4612030, A4542015, A4602014, A4602026, A4622036, A5522045, A5532047, A4612033, A5512040, A4612032, A4562003, A4572004, A4592012, A4562018, A4622035, A4522009, A4602025, A3582001, A5512043, A45320 11, A4602024, A5512018, A4572006, A4572023, A5512019, A5532049, A3592002, A4602027, A4552002, A4512006, A4552017, A5522046, A4572005, A4562019, A4572021, A4522008, A4612034, A4582009, A3612004, A4622016, A4532010, A3622001, A5512044, A4552016, A4572007, A4592011, A4572008, & A5512042
Products Sold
Serial Numbers: A4622037, A4612031, A4622017, A4532013, A4582010, A5532048, A4592013, A4532012, A5532022, A4602028, A3592003, A4522007, A5512041, A4612015, A4572020, A4602029, A4622039, A4612030, A4542015, A4602014, A4602026, A4622036, A5522045, A5532047, A4612033, A5512040, A4612032, A4562003, A4572004, A4592012, A4562018, A4622035, A4522009, A4602025, A3582001, A5512043, A45320 11, A4602024, A5512018, A4572006, A4572023, A5512019, A5532049, A3592002, A4602027, A4552002, A4512006, A4552017, A5522046, A4572005, A4562019, A4572021, A4522008, A4612034, A4582009, A3612004, A4622016, A4532010, A3622001, A5512044, A4552016, A4572007, A4592011, A4572008, & A5512042
Toshiba American Med Sys Inc is recalling Toshiba Excelart VANTAGE Model MRT-1503, Magnetic Resonance Imaging Systems, Regulation Number 21 CP due to To correct a hardware problem of water leakage in the cooling system inside the ASGC, leading to the replacement of the gradient coil.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
To correct a hardware problem of water leakage in the cooling system inside the ASGC, leading to the replacement of the gradient coil.
Recommended Action
Per FDA guidance
Toshiba America Medical Systems, Inc., (TAMS) customer service engineers will hand deliver The Advisory Letter and monitor the system during their monthly preventive maintenance.
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