Philips Respironics, Inc. recalls BiPAP A30 Ventilators. Intended to provide noninvasive ventilation support in adult and…
This device does not indicate for use in patients with respiratory failure.
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 481–492 of 581 recalls
This device does not indicate for use in patients with respiratory failure.
This device does not indicate for use in patients with respiratory failure.
In very rare situations, communication between the sensor measuring dose applied to the area and the corresponding software fails.…
In very rare situations, communication between the sensor measuring dose applied to the area and the corresponding software fails.…
In very rare situations, communication between the sensor measuring dose applied to the area and the corresponding software fails.…
In very rare situations, communication between the sensor measuring dose applied to the area and the corresponding software fails.…
A resistor in the frequency inverter may strongly overheat potentially igniting the plastic housing of the frequency inverter on fire.
A resistor in the frequency inverter may strongly overheat potentially igniting the plastic housing of the frequency inverter on fire.
Potential for thermal incident including an unexpected occurrence of smoke, sparks, burning, or unsteady flames during clinical use.…
Potential for thermal incident including an unexpected occurrence of smoke, sparks, burning, or unsteady flames during clinical use.…
Potential for thermal incident including an unexpected occurrence of smoke, sparks, burning, or unsteady flames during clinical use.…
Potential for thermal incident including an unexpected occurrence of smoke, sparks, burning, or unsteady flames during clinical use.…