Aesculap Implant Systems LLC: Medical Device Recall in 2022 - (Recall #: Z-1516-2022)

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:

Aeos¿ Robotic Digital Microscope with software versions 2.7 or earlier Article Number: PV010

Product Classification:

Class II

Date Initiated: July 14, 2022

Date Posted: August 17, 2022

Recall Number: Z-1516-2022

Event ID: 90641

Reason for Recall:

Application error problems: Rebalance scope message: 1.Rebalancing process 2.Usage of Robot Recovery: 3. Autofocus not available:

Status: Terminated

Product Quantity: 5 units

Code Information:

GUIDID: 04046955206742 Serial Numbers: 1004; 1026; 1032; 1035; 1036

Distribution Pattern:

US Distribution to states of: AR, IN, NE and NC

Voluntary or Mandated:

Voluntary: Firm initiated