# FDA recall Z-1516-2022

> **Aesculap Implant Systems LLC** · Class II · device recall initiated 2022-07-14.

## 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:

## Distribution

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

## Key facts

- **Recall number:** Z-1516-2022
- **Recalling firm:** Aesculap Implant Systems LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-07-14
- **Report date:** 2022-08-17
- **Termination date:** 2025-02-07

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Center Valley, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1516-2022

## Citation

> AI Analytics. FDA recall Z-1516-2022. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1516-2022. Source: US FDA. Licensed CC0.

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