Skip to content
Recall Observatory FDA recall evidence

Device product

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

Z-1516-2022

July 14, 2022

Class II

Product summary

Firm
Aesculap Implant Systems LLC
Event
Event 90641
Status
Terminated
Classification
Class II
Quantity
5 units
Official record key
device-enforcement:Z-1516-2022

Official wording

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

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

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

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

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