HIGHFDA DEVICE
Maquet Cardiopulmonary Recalls Venous Bubble Sensor Due to Cable Risk
Maquet Cardiopulmonary Gmbh recalled 3,050 Venous Bubble Sensors on January 9, 2026. Internal investigations revealed issues with the durability of the connecting cable. Excessive bending can lead to device failure, posing a risk to patient safety.
Maquet Cardiopulmonary Gmbh
Internal investigations