Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 205–216 of 262 recalls
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.
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.
When following a specific less typical workflow in which the user remeasures using the ultrasound device or manually edits primitive or derived measurement values directly in Clinical Reporting, derived measurements may…
When following a specific less typical workflow in which the user remeasures using the ultrasound device or manually edits primitive or derived measurement values directly in Clinical Reporting, derived measurements may…