RMU-2000 Automated Chest Compression Device
Reported: August 21, 2024 Initiated: July 12, 2024 #Z-2543-2024
Product Description
RMU-2000 Automated Chest Compression Device
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.
Details
- Recalling Firm
- Defibtech, LLC
- Units Affected
- 174 US, 37 OUS
- Distribution
- Domestic distribution to CT, FL, NJ, SC, TN. Foreign distribution to Japan
- Location
- Guilford, CT
Frequently Asked Questions
What product was recalled? ▼
RMU-2000 Automated Chest Compression Device. Recalled by Defibtech, LLC. Units affected: 174 US, 37 OUS.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 21, 2024. Severity: Critical. Recall number: Z-2543-2024.
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