Product Description
FDR Visionary Suite;
Model Number: CH-200;
Version: (1) 566-16130-23, (2) 566-16130-31, (3)
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.
Action Details
On January 9, 2026 URGENT: MEDICAL DEVICE RECALL letters were emailed to customers. Actions to be taken:
Please pay attention to the following points until the work is completed.
" For safety reasons, please turn off the breaker of the distribution board to which the power cord of the unit is connected after turning off the power of the unit according to the operation manual.
" Do not forget to turn off the breaker of the distribution board until the replacement of the contactor is completed.
1) Please post this notification on or near the device
2) Please complete and return the Field Action Verification Form attached to this communication. Responding with the information requested is essential for ensuring appropriate action is taken.
3) Please contact Technical Assistance Center (TAC) at 1-888-FUJIMED (1-888-385-4633) to open a service ticket.
4) Please report any known adverse events to FDA via MedWatch.
Distribution Pattern
US Nationwide distribution in the states of AK, CA, CT, FL, IL, NH, OH, WI.
Code Information / Serial Numbers
Model Number: CH-200;
(1) Version: 566-16130-23;
UDI-DI: 04540217052226;
Serial numbers: MP95A9F6A001, MP95A9F6B001, MP95A9F74001, MP95A9F74002, MP95A9F76001, MP95A9F78001;
(2) Version: 566-16130-31;
UDI-DI: 04540217057436;
Serial numbers: MP95AA783001;
(3) Version: 566-16130-33;
UDI-DI: 04540217057450;
Serial numbers: MP95AA983001, MP95AA983002, MP95AA983003, MP95AA985001, MP95AA985003, MP95AA985002, MP95AA988001, MP95AA988002;
Public Record Disclaimer
This page represents an index of public-record FDA device recalls. It does not imply current safety or compliance status of the product. AvaSpecs is a private aggregator and is not affiliated with the FDA or any government agency. This page does not constitute medical, safety, legal, regulatory, or compliance advice. Refer to official government sources for primary safety alerts.