FDA Device recall Z-1516-2022
Aeos¿ Robotic Digital Microscope with software versions 2.7 or earlier Article Number: PV010
- FDA Device
- Class II
- terminated
- Published 2022-08-17
On 2022-08-17 the FDA classified a Class II recall of Aeos¿ Robotic Digital Microscope with software versions 2.7 or earlier Article Number: PV010 by Aesculap Implant Systems, citing application error problems: Rebalance scope message: 1.Rebalancing process 2.Usage of Robot Recovery: 3. Autofocus not available:.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1516-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-07-14 |
| Published | 2022-08-17 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Aesculap Implant Systems |
| Distribution | AR, IN, NC, NE |
Product
Aeos¿ Robotic Digital Microscope with software versions 2.7 or earlier Article Number: PV010
Reason
Application error problems: Rebalance scope message: 1.Rebalancing process 2.Usage of Robot Recovery: 3. Autofocus not available:
Identifiers
| code_info | GUIDID: 04046955206742 Serial Numbers: 1004; 1026; 1032; 1035; 1036 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1516-2022%22
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