Olympus Corporation Of The Americas recalls Olympus High Flow Insufflation Unit. Model Number: UHI-3. Used for insufflation of…
Issue with software algorithm which may lead to overpressure events.
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 85–96 of 119 recalls
Issue with software algorithm which may lead to overpressure events.
Issue with software algorithm which may lead to overpressure events.
Issue with software algorithm which may lead to overpressure events.
Devices which did not undergo thermoforming could deform and lose performance.
Devices which did not undergo thermoforming could deform and lose performance.
Devices which did not undergo thermoforming could deform and lose performance.
Devices which did not undergo thermoforming could deform and lose performance.
Devices which did not undergo thermoforming could deform and lose performance.
Devices which did not undergo thermoforming could deform and lose performance.
Devices which did not undergo thermoforming could deform and lose performance.
Devices which did not undergo thermoforming could deform and lose performance.
Devices which did not undergo thermoforming could deform and lose performance.