PlainRecalls
FDA Devices Moderate Class II Terminated

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

Reported: August 17, 2022 Initiated: July 14, 2022 #Z-1516-2022

Product Description

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

Reason for Recall

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

Details

Units Affected
5 units
Distribution
US Distribution to states of: AR, IN, NE and NC
Location
Center Valley, PA

Frequently Asked Questions

What product was recalled?
Aeos¿ Robotic Digital Microscope with software versions 2.7 or earlier Article Number: PV010. Recalled by Aesculap Implant Systems LLC. Units affected: 5 units.
Why was this product recalled?
Application error problems: Rebalance scope message: 1.Rebalancing process 2.Usage of Robot Recovery: 3. Autofocus not available:
Which agency issued this recall?
This recall was issued by the FDA Devices on August 17, 2022. Severity: Moderate. Recall number: Z-1516-2022.