Aeos Robotic Digital Microscope — Class II medical device recall Z-2139-2024
Ongoing recall by Aesculap Inc, reported 2024-06-19, distributed nationwide. Possibility of the robotic arm to drop more than 10cm from its original position after pressing the emergency
| Recall number | Z-2139-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Aesculap Inc, Center Valley, PA, United States |
| Recall initiated | 2024-05-13 |
| Classified | 2024-06-12 |
| Reported by FDA | 2024-06-19 |
| Distributed | Nationwide (US) |
| Quantity | 19 units |
| UPC / GTIN / UDI-DI | 04046955206742 |
| Serial numbers | 1004, 1005, 1011, 1026, 1027, 1032, 1035, 1036, 1038, 1054, 1056, 1057, 1060, 1061, 1063, 1084, 1089, 1093, 1097 |
Product
Aeos Robotic Digital Microscope, Product Code: PV010
Reason for recall
Possibility of the robotic arm to drop more than 10cm from its original position after pressing the emergency stop button due to failure of the integrated safety mechanism.
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-2139-2024. 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.