Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0644-2016 — 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 M

U.S. FDA — Device Enforcement · United States · 2015-12-04 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0644-2016
Date of alert: 2015-12-04
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: CompView Medical, LLC
Product category: device
Product type: Devices

Reported risk: 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.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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