---
title: "Aeos¿ Robotic Digital Microscope with software versions 2.7 or earlier Articl... — FDA record Z-1516-2022 | Is It on Recall"
description: "Application error problems: Rebalance scope message: 1.Rebalancing process 2.Usage of Robot Recovery: 3. Autofocus not available:"
url: https://isitonrecall.com/recall/fda-device-z-1516-2022-aeos-robotic-digital-microscope-with-software-versions-2-7-or-earlier-article-number-pv010/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Aeos¿ Robotic Digital Microscope with software versions 2.7 or earlier Article Number: PV010 — FDA record Z-1516-2022

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jul 14, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **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:
- **Classification**: Class II
- **Recalling firm**: Aesculap Implant Systems LLC
- **Quantity**: 5 units
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-1516-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1516-2022%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | GUIDID: 04046955206742 Serial Numbers: 1004; 1026; 1032; 1035; 1036 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US Distribution to states of: AR, IN, NE and NC

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Arkansas](https://isitonrecall.com/state/arkansas/)
- [Indiana](https://isitonrecall.com/state/indiana/)
- [North Carolina](https://isitonrecall.com/state/north-carolina/)
- [Nebraska](https://isitonrecall.com/state/nebraska/)

## Dates in the source

- **Report date**: Aug 17, 2022
- **Recall initiation date**: Jul 14, 2022
- **Center classification date**: Aug 11, 2022
- **Termination date**: Feb 7, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1516-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Aesculap Implant Systems LLC records](https://isitonrecall.com/brand/aesculap-implant-systems-llc/)