Medical Device Recall: FDR Visionary Suite; Model Number: CH-200; Version: (1) 566-16130-23, (2) 566-16130-31, (3)
FUJIFILM Healthcare Americas Corporation · January 9, 2026
Reason for Recall
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.
Distribution
US Nationwide distribution in the states of AK, CA, CT, FL, IL, NH, OH, WI.
States Affected
NATIONWIDE
Quantity Affected
16 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1299-2026
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.