The FDA has posted 5 enforcement recalls of radiologic table devices since 2025, none of them Class I (most serious). Most recent report: Apr 2, 2025.
There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
Source: U.S. FDA openFDA device enforcement reports, updated continuously. Device type per the FDA's RES classification (“Table, Radiologic”). Informational only — verify against the FDA before acting.