Recall
Aeos Robotic Digital Microscope, Product Code: PV010
Aesculap Inc · 13 May 2024
- Status
- Recall open, classified
- Why, in the FDA's words
- “Possibility of the robotic arm to drop more than 10cm from its original position after pressing the emergency stop button due to failure of the integrated safety mechanism.”
- Recall began
- 13 May 2024
- Company
- Aesculap Inc
- 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.