Recall
Aeos Robotic Digital Microscope with software versions 2.7 or earlier Article Number: PV010
Aesculap Implant Systems LLC · 14 July 2022
- Status
- Recall terminated
- Why, in the FDA's words
- “Application error problems: Rebalance scope message: 1.Rebalancing process 2.Usage of Robot Recovery: 3. Autofocus not available:”
- Recall began
- 14 July 2022
- Company
- Aesculap Implant Systems LLC
- Device type
- Product code (FSO)
What it means
A recall is the FDA's record that a company is correcting or removing a device because of a problem. Many are fixed with a software update or new instructions; the record does not say whether anyone was hurt. See our plain guide to FDA terms.
The record
The FDA publishes this record in its public device database. The summary documents the company filed, when available, are linked from the FDA's page.