Defibtech, LLC recalls RMU-2000 Automated Chest Compression Device

Recalled August 21, 2024 · FDA recall Z-2543-2024 · Defibtech

Hazard

Problem in the device's motor may cause the device to stop compressions. This may lead to a delay in therapy if the device fails to operate, and could lead to patient injury or death. · FDA Class I

Units

174 US, 37 OUS

Sold at

Domestic distribution to CT, FL, NJ, SC, TN. Foreign distribution to Japan

Description

Problem in the device's motor may cause the device to stop compressions. This may lead to a delay in therapy if the device fails to operate, and could lead to patient injury or death.

Product

RMU-2000 Automated Chest Compression Device

Manufacturer(s)

Defibtech, LLC

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →