⚠ Recalls found. Brand Name is named in 2 official recalls in our current data:
FDA Class II recall Z-2310-2026 — Due to unintentionally activated near infrared handheld camera when attempting to turn off illumination during normal clinical workflow transitions, particularly when switching from the handheld camera to the robotic endoscope.
FDA Class II recall Z-2046-2026 — Due to manipulator containing screws with in the arm sub-assembly that my be susceptible to breaking.
Due to unintentionally activated near infrared handheld camera when attempting to turn off illumination during normal clinical workflow transitions, particularly when switching fro…