Hamilton Medical Corrects C6 Ventilators Over Circuit Board Defect
The FDA has issued a Class I recall designation for the correction, which addresses a fault that can cause ventilation to stop unexpectedly.
The FDA has issued a Class I recall designation for the correction, which addresses a fault that can cause ventilation to stop unexpectedly.
Baxter is recalling certain Volara System components due to a disconnection issue that may lead to insufficient ventilation.
Hamilton Medical AG is recalling an intensive care ventilator after complaints revealed a hardware issue with its status indicator board.
The FDA has issued a Class I recall designation for the correction, which addresses a fault that can cause ventilation to stop unexpectedly.