Aesculap Implant Systems LLC: Medical Device Recall in 2022 - (Recall #: Z-1409-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

Universal Robot UR5 arm, PV010204 subcomponent of Aesculap Aeos Digital Microscope System, PV010

Product Classification:

Class II

Date Initiated: February 19, 2021

Date Posted: July 27, 2022

Recall Number: Z-1409-2022

Event ID: 90532

Reason for Recall:

Malfunction of the robotic arm preventing further movement of the robotic arm and requiring restart of the robotic digital microscope system.

Status: Completed

Product Quantity: 1

Code Information:

UDI-DI: 04046955206742, Serial Number: SN1004

Distribution Pattern:

United States: NE

Voluntary or Mandated:

Voluntary: Firm initiated