Recall Z-2139-2024— Aesculap Inc
Class II · Ongoing
Class II FDA medical device recall by Aesculap Inc, initiated 2024-05-13. FDA's recall record names no specific 510(k) clearance for this event. Product: Aeos Robotic Digital Microscope, Product Code: PV010. Reason: 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..
- Recalling firm
- Aesculap Inc
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2024-05-13
- Firm location
- Center Valley, PA, United States
Product description
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.