FUJIFILM Healthcare recalls specific models of X-ray high-voltage generators (CH-200) due to risk of overheating and smoke after power cut. Affected units have unique serial numbers and versions.
It was found that the contacts of the electromagnetic contactors used inside the cabinet of the X-ray high-voltage generator were welded, and the current might continue to be supplied to the power supply circuit even if the power of the device is cut off. As a result, it cannot be denied that the circuit in question overheats and damages the surrounding parts. It may also cause smoke.
FUJIFILM Healthcare is recalling certain X-ray high-voltage generators (FDR Visionary Suite CH-200) because internal electrical contacts can weld, causing overheating and potential smoke even after power is turned off. This poses a fire risk if the device is used improperly.
The electromagnetic contactors inside the X-ray generator can weld, allowing electricity to continue flowing even when the device is powered off. This causes the circuit to overheat, potentially damaging parts and producing smoke.
Healthcare facilities using the FDR Visionary Suite CH-200 X-ray generators with specific model numbers and versions are most at risk. Patients and staff could be exposed to smoke or fire if the device malfunctions.
Check for the model number CH-200 and specific versions: 566-16130-23, 566-16130-31, or 566-16130-33. Affected units have unique serial numbers listed in the recall notice.
Identify the model number (CH-200) and version numbers (566-16130-23, 566-16130-31, or 566-16130-33) on your X-ray generator.
If your device matches the recalled model and version, stop using it immediately to prevent overheating or smoke.
The electromagnetic contactors inside the X-ray generator can weld, causing electricity to continue flowing even when powered off. This leads to overheating and potential smoke.
Check for model number CH-200 and specific versions: 566-16130-23, 566-16130-31, or 566-16130-33. Affected units have unique serial numbers listed in the recall notice.
Stop using it immediately and contact FUJIFILM Healthcare for further instructions.
We’ve drafted a message you can send FUJIFILM Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-1299-2026 — FUJIFILM Healthcare FUJIFILM Healthcare Hello, I own a FUJIFILM Healthcare that is covered by recall Z-1299-2026 from FUJIFILM Healthcare. 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.
