Recall
Universal Robot UR5 arm, PV010204 subcomponent of Aesculap Aeos Digital Microscope System, PV010
Aesculap Implant Systems LLC · 19 Feb 2021
- Status
- Recall completed
- Why, in the FDA's words
- “Malfunction of the robotic arm preventing further movement of the robotic arm and requiring restart of the robotic digital microscope system.”
- Recall began
- 19 Feb 2021
- 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.