Aesculap Inc: Medical Device Recall in 2024 - (Recall #: Z-2139-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Aeos Robotic Digital Microscope, Product Code: PV010

Product Classification:

Class II

Date Initiated: May 13, 2024

Date Posted: June 19, 2024

Recall Number: Z-2139-2024

Event ID: 94623

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.

Status: Ongoing

Product Quantity: 19 units

Code Information:

Product Code: PV010, UDI/DI: 04046955206742; Serial Numbers: 1011, 1005, 1057, 1032, 1038, 1054, 1036, 1060, 1056, 1089, 1093, 1027, 1061, 1004, 1026, 1035, 1097, 1084, 1063

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated