Class 1 FDA Recall on Chest Compression Device – What You Need to Know
Oliver
September 6, 2024
The FDA has issued a recall on the RMU-2000 ARM XR chest compression device created by Defibtech. The purpose of this technology is to maintain oxygenated blood throughout the body. Chest compressions are crucial during cardiac emergencies. A malfunctioning device can significantly endanger a patient’s life. The notice reports an
