FDA Device recall Z-1409-2022
Universal Robot UR5 arm, PV010204 subcomponent of Aesculap Aeos Digital Microscope System, PV010
- FDA Device
- Class II
- completed
- Published 2022-07-27
On 2022-07-27 the FDA classified a Class II recall of Universal Robot UR5 arm, PV010204 subcomponent of Aesculap Aeos Digital Microscope System, PV010 by Aesculap Implant Systems, citing malfunction of the robotic arm preventing further movement of the robotic arm and requiring restart of the robotic digital microscope system.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1409-2022 |
| Classification | Class II |
| Status | completed |
| Initiated | 2021-02-19 |
| Published | 2022-07-27 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Aesculap Implant Systems |
| Distribution | NE |
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.
Identifiers
| code_info | UDI-DI: 04046955206742, Serial Number: SN1004 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: completed.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1409-2022%22
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