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Home » Do Not Use Recalled Chest Compression Device, FDA Warns

Do Not Use Recalled Chest Compression Device, FDA Warns

August 26, 2024
Devices Regulatory Affairs
Debfitech has issued an urgent medical device safety removal letter to its customers of the RMU-2000 ARM XR chest compression device, which provides chest compressions on adults whose hearts suddenly stop, directing that the device be removed from use.

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