Recall Z-1409-2022— Aesculap Implant Systems LLC
Class II · Completed
Class II FDA medical device recall by Aesculap Implant Systems LLC, initiated 2021-02-19. FDA's recall record names no specific 510(k) clearance for this event. Product: Universal Robot UR5 arm, PV010204 subcomponent of Aesculap Aeos Digital Microscope System, PV010. Reason: Malfunction of the robotic arm preventing further movement of the robotic arm and requiring restart of the robotic digital microscope system..
- Recalling firm
- Aesculap Implant Systems LLC
- Classification
- Class II
- Status
- Completed
- Initiated
- 2021-02-19
- Firm location
- Center Valley, PA, United States
Product description
Universal Robot UR5 arm, PV010204 subcomponent of Aesculap Aeos Digital Microscope System, PV010
Reason for recall
Malfunction of the robotic arm preventing further movement of the robotic arm and requiring restart of the robotic digital microscope system.
Data sourced from openFDA. This site is unofficial and independent of the FDA.