Aesculap Inc: Device Recall

Recall #Z-2139-2024 · 05/13/2024

Class II: Risk

Recall Details

Recall Number: Z-2139-2024
Classification: Class II
Product Type: Device
Recalling Firm: Aesculap Inc
Status: Ongoing
Date Initiated: 05/13/2024
Location: Center Valley, PA, United States
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 19 units

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.

Product Description

Aeos Robotic Digital Microscope, Product Code: PV010

Distribution Pattern

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

Other Recalls by Aesculap Inc

Class II: Risk 09/24/2025

It was determined there is the potential of silicone fragments detaching from the yellow sealing component.
Class II: Risk 09/24/2025

It was determined there is the potential of silicone fragments detaching from the yellow sealing component.
Class II: Risk 09/24/2025

It was determined there is the potential of silicone fragments detaching from the yellow sealing component.
Class II: Risk 09/24/2025

It was determined there is the potential of silicone fragments detaching from the yellow sealing component.
Class II: Risk 01/31/2025

The forceps have been used in ways not covered by the design resulting in breakage of the clamps.

View all recalls by Aesculap Inc →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.