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Recall Observatory FDA recall evidence

Device product

Universal Robot UR5 arm, PV010204 subcomponent of Aesculap Aeos Digital Microscope System, PV010

Z-1409-2022

February 19, 2021

Class II

Product summary

Firm
Aesculap Implant Systems LLC
Event
Event 90532
Status
Completed
Classification
Class II
Quantity
1
Official record key
device-enforcement:Z-1409-2022

Official wording

Reason: Malfunction of the robotic arm preventing further movement of the robotic arm and requiring restart of the robotic digital microscope system.

Code information: UDI-DI: 04046955206742, Serial Number: SN1004

Distribution pattern: United States: NE

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Malfunction of the robotic arm preventing further movement of the robotic arm and requiring restart of the robotic digital microscope system.

Field note

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