Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
RMU-2000 Automated Chest Compression Device Recalled by Defibtech, LLC Due to Problem in the device's motor may cause the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Defibtech, LLC directly.
Affected Products
RMU-2000 Automated Chest Compression Device
Quantity: 174 US, 37 OUS
Why Was This 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.
Where Was This Sold?
This product was distributed to 5 states: CT, FL, NJ, SC, TN
About Defibtech, LLC
Defibtech, LLC has 14 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report