Defibtech is recalling its RMU-2000 ARM XR Chest Compression Device.
The recall is in response to a problem with the device’s motor that causes chest compressions to stop, which has resulted in one injury and one death, according to an Aug. 22 news release from the FDA.
Users are instructed to identify and cease use of the affected devices. Defibtech said it will contact customers for returns, refunds or replacements.
Read the full list of serial numbers for affected devices here.
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