Aeos¿ Robotic Digital Microscope with software versions 2 — Class II medical device recall Z-1516-2022
Terminated recall by Aesculap Implant Systems LLC, reported 2022-08-17, distributed in AR, IN, NC, NE. Application error problems: Rebalance scope message: 1.Rebalancing process 2.Usage of Robot Recovery: 3. Autof
| Recall number | Z-1516-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Aesculap Implant Systems LLC, Center Valley, PA, United States |
| Recall initiated | 2022-07-14 |
| Classified | 2022-08-11 |
| Reported by FDA | 2022-08-17 |
| Terminated | 2025-02-07 |
| Distributed | AR, IN, NC, NE |
| Quantity | 5 units |
| UPC / GTIN / UDI-DI | 04046955206742 |
| Serial numbers | 1004, 1026, 1032, 1035, 1036 |
Product
Aeos¿ Robotic Digital Microscope with software versions 2.7 or earlier Article Number: PV010
Reason for recall
Application error problems: Rebalance scope message: 1.Rebalancing process 2.Usage of Robot Recovery: 3. Autofocus not available:
Machine access
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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.