Class II
Medical Device Recall: Aeos Robotic Digital Microscope, Product Code: PV010
Aesculap Inc · May 13, 2024
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.
States Affected
NATIONWIDE
Quantity Affected
19 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2139-2024
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.