# FDA recall Z-2139-2024

> **Aesculap Inc** · Class II · device recall initiated 2024-05-13.

## 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.

## Distribution

US Nationwide distribution in the states of AR, FL, IL, IN, KY, MI, NC, NE, OK, SD, TX.

## Key facts

- **Recall number:** Z-2139-2024
- **Recalling firm:** Aesculap Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-05-13
- **Report date:** 2024-06-19

- **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-2139-2024

## Citation

> AI Analytics. FDA recall Z-2139-2024. Retrieved 2026-05-24 from https://api.ai-analytics.org/recall/Z-2139-2024. Source: US FDA. Licensed CC0.

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