TOSHIBA SUPERCONDUCTING MRI SYSTEM Vantage TitanRecalls & reported problems across all models

We found 2 models of TOSHIBA SUPERCONDUCTING MRI SYSTEM Vantage Titan by Canon Inc. in the FDA's device registry (GUDID). Together they are named in 1 adverse event report in the FDA's MAUDE database, received between Jan 5, 2026 and Jan 5, 2026 — classified as 1 injury.

The most frequently reported specific device problem is “Patient Device Interaction Problem” (1 report).

2 FDA recall records name at least one of these models by its device identifier, 2 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

TOSHIBA SUPERCONDUCTING MRI SYSTEM Vantage Titan recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

1. May 10, 2024Class IIOpen, Classified

   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.

   Z-2041-2024 · Root cause: Device Design · Recall details · FDA record ↗

2. Jan 29, 2024Class IIOpen, Classified

   For some MRI systems, it has been found that some of the maximum Spatial Field Gradient (SFG) values displayed in "System Information" of the operation window and some of the maximum SFG values described in the safety manual are lower than the correct values, which may cause a patient with an MR conditional device to feel some discomfort during the MR scan.

   Z-1250-2024 · Root cause: Component change control · Recall details · FDA record ↗

Most reported TOSHIBA SUPERCONDUCTING MRI SYSTEM Vantage Titan problems

TOSHIBA SUPERCONDUCTING MRI SYSTEM Vantage Titan models

2 models, most reported first. Each model has its own page with its reports, recalls and device details.

• TOSHIBA SUPERCONDUCTING MRI SYSTEM Vantage Titan MRT-1504

  System, nuclear magnetic resonance imaging
  2 recalls0 reports
• TOSHIBA SUPERCONDUCTING MRI SYSTEM Vantage Titan MRT-1510

  System, nuclear magnetic resonance imaging
  1 report

Recent TOSHIBA SUPERCONDUCTING MRI SYSTEM Vantage Titan adverse event reports

The 1 most recent reports across all models, in the reporter's own words as published by the FDA.

• InjuryJan 5, 2026Patient Device Interaction Problem

  IT WAS REPORTED THAT ON (B)(6) 2025, A PATIENT RECEIVED A BURN COMPATIBLE WITH THEIR RIGHT LOWER EXTREMITY (RLE) RESTING AGAINST DIACOR MR-TEK350 STAINLESS STEEL PORTION OF STIRRUP. THE PATIENT UNDERWENT EPIDURAL FOR HIGH DOSE RADIATION (HDR) PROCEDURE WHICH REQUIRED PATIENT'S BILATERAL LOWER EXTREMITIES TO BE POSITIONED IN DIACOR STIRRUPS. THE PATIENT WAS TAKEN TO MRI FOR VERIFICATION OF NEEDLE PLACEMENT. FOLLOWING HDR PROCEDURE NURSING STAFF NOTICED WOUND TO PATIENT'S RIGHT OUTER THIGH. AREA WAS RED WITH A LARGE WHITE/BLANCHED AREA IN THE CENTER RESEMBLING A BURN. THE PATIENT RETURNED FOR THEIR 1-WEEK FOLLOW-UP FOR THE HDR PROCEDURE AND REPORTED WORSENING OF WOUND. THE PATIENT REQUIRED CARE AT ADVANCED WOUND CARE CENTER. PER MRI SAFETY OFFICER PATIENT EXPERIENCED "MRI BURN" FROM TOUCHPOINT OF RLE WITH STAINLESS STEEL COMPONENT OF ZEPHYR STIRRUP HINGE. THE PATIENT LIKELY DID NOT EXPERIENCE SENSATION OF "BURN" OR PRESSURE DURING MRI TESTING DUE TO THE EPIDURAL RECEIVED FOR THE HDR PROCEDURE. THIS REPORTED INCIDENT (MW5180429) WAS RECEIVED BY CANON VIA THE FDA'S MEDWATCH PROGRAM.

  Patient problems: Burn(s)

  MAUDE report 23962290 ↗

Other Canon Inc. products

• INTERVENTIONAL ANGIOGRAPHY SYSTEM3 models · 6 reports · 5 recalls
• DIAGNOSTIC ULTRASOUND SYSTEM5 models · 1 reports · 1 recall