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Aesculap Implant Systems LLC recalls Universal Robot UR5 arm, PV010204 subcomponent of Aesculap Aeos Digital Microscope System, PV010
Recalled July 27, 2022 · FDA recall Z-1409-2022 · Aesculap Implant Systems
Hazard
Malfunction of the robotic arm preventing further movement of the robotic arm and requiring restart of the robotic digital microscope system. · FDA Class II
Units
1
Sold at
United States: NE
Description
Malfunction of the robotic arm preventing further movement of the robotic arm and requiring restart of the robotic digital microscope system.
Product
Universal Robot UR5 arm, PV010204 subcomponent of Aesculap Aeos Digital Microscope System, PV010
Manufacturer(s)
Aesculap Implant Systems LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →