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FDAFebruary 19, 2021device

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

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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

What to do

FDA enforcement status: Completed

Brands named

aesculap implant systemsaesculapaesculap implant

UPCs

04046955206742

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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