Class I

Medical Device Recall: RMU-2000 Automated Chest Compression Device

Defibtech, LLC · July 12, 2024

Reason for Recall

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.

Distribution

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

States Affected

CT, FL, NJ, SC, TN

Quantity Affected

174 US, 37 OUS

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2543-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.