Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Model NuCARTGN. The NuCART is a mobile display and image Recalled by CompView Medical, LLC Due to The attachment of the NuCART Spring Arm to...
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 CompView Medical, LLC directly.
Affected Products
Model NuCARTGN. The NuCART is a mobile display and image management platform used in Minimally Invasive Surgery (MIS) environments to facilitate the routing and ergonomic display of video signals from source devices to flat-panel monitors. It is tailored for use with an OEC C-arm and Endo-Cam in MIS surgery suites, Ambulatory Surgery Centers, Urology, GI and other suites.
Quantity: 10 units
Why Was This Recalled?
The attachment of the NuCART Spring Arm to the NuCART horizontal boom may come apart if the securing ring (snap ring) was not installed correctly causing the spring arm to release and detach.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About CompView Medical, LLC
CompView Medical, LLC has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report