Universal Robot UR5 arm — Class II medical device recall Z-1409-2022
Completed recall by Aesculap Implant Systems LLC, reported 2022-07-27. Malfunction of the robotic arm preventing further movement of the robotic arm and requiring restart of the rob
| Recall number | Z-1409-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | Aesculap Implant Systems LLC, Center Valley, PA, United States |
| Recall initiated | 2021-02-19 |
| Classified | 2022-07-19 |
| Reported by FDA | 2022-07-27 |
| Quantity | 1 |
| Reason classes | device malfunction |
| UPC / GTIN / UDI-DI | 04046955206742 |
| Serial numbers | SN1004 |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1409-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.