Shimadzu recalls specific FLUOROspeed X-ray systems that may fail to display images when switching modes, potentially delaying or canceling medical exams. Affected units have unique serial numbers.
X-ray R/F system software with certain versions of the control board may occasionally fail to display images when switching from Fluoroscopy mode to Radiography mode, which may lead to the possibility of delay or cancellation of the examination.
Shimadzu is recalling certain FLUOROspeed X-ray systems that may fail to display images when switching from fluoroscopy to radiography mode. This could delay or cancel medical exams if the system doesn't show images properly during the switch.
The software on the control board may occasionally fail to display images when switching from fluoroscopy to radiography mode. This could cause delays or cancellations of medical exams if the system doesn't show images properly during the switch.
Medical facilities using the recalled FLUOROspeed systems, particularly those performing radiographic or fluoroscopic exams. Patients undergoing these procedures may be affected if the system fails to display images during the switch.
Check for serial numbers starting with MQ493E3D or MQ493E3E followed by specific digits listed in the recall notice. The FLUOROspeed is used for radiographic and fluoroscopic imaging in medical settings.
Verify if your FLUOROspeed has a serial number starting with MQ493E3D or MQ493E3E followed by specific digits listed in the recall notice.
The software on the control board may occasionally fail to display images when switching from fluoroscopy to radiography mode, which could delay or cancel medical exams.
Check for serial numbers starting with MQ493E3D or MQ493E3E followed by specific digits listed in the recall notice.
The recall does not specify a remedy, so contact Shimadzu directly for further instructions.
We’ve drafted a message you can send Shimadzu to request your refund or repair — edit it as you like.
Subject: Recall Z-0317-2025 — Shimadzu Shimadzu Hello, I own a Shimadzu that is covered by recall Z-0317-2025 from Shimadzu. 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.
