Shimadzu Medical Systems recalls Digital Angiography Systems Trinias:UD150G-40 / D150GC-40 and BRANSIST safire:UD150G-40 models due to risk of current supply even when power is off. Affected units have specific serial numbers listed in the recall.
Electromagnetic contactors within high voltage generator may weld together, resulting in current being supplied to power supply even if power is off.
Shimadzu Medical Systems is recalling several digital angiography and radiography systems because electromagnetic contactors inside the high-voltage generator may weld together, causing power to be supplied even when the system is turned off. This could lead to unintended operation or damage.
Electromagnetic contactors within the high-voltage generator can weld together, causing the system to supply power even when it's turned off. This may lead to unintended operation or damage but does not pose an immediate risk of injury or death.
Healthcare facilities and medical professionals who own or use the affected Shimadzu Digital Angiography Systems Trinias:UD150G-40 / D150GC-40 and BRANSIST safire:UD150G-40 models. The risk is low as the hazard is specific to certain units with listed serial numbers.
Check if your system has the model numbers listed: Trinias:UD150G-40 / D150GC-40 or BRANSIST safire:UD150G-40. Affected units have specific serial numbers from the list provided in the recall.
Verify if your system matches the model numbers listed in the recall: Trinias:UD150G-40 / D150GC-40 or BRANSIST safire:UD150G-40.
If your system is affected, contact Shimadzu Medical Systems directly for further instructions.
The affected models are Shimadzu Digital Angiography Systems Trinias:UD150G-40 / D150GC-40 and BRANSIST safire:UD150G-40.
Check if your system has the model numbers listed in the recall: Trinias:UD150G-40 / D150GC-40 or BRANSIST safire:UD150G-40. Affected units have specific serial numbers from the list provided in the recall.
The hazard is specific to certain units with listed serial numbers and does not pose an immediate risk of injury or death. The risk is low as the issue may cause unintended operation but not direct harm.
We’ve drafted a message you can send Shimadzu Medical Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-2294-2026 — Shimadzu Medical Systems Shimadzu Medical Systems Hello, I own a Shimadzu Medical Systems that is covered by recall Z-2294-2026 from Shimadzu Medical Systems. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
