Recall
CORI REAL INTELLIGENCE Robotic Drill, Product No. ROB10013 and ROB10013S
Blue Belt Technologies, Inc · 13 Nov 2023
- Status
- Recall open, classified
- Why, in the FDA's words
- “Possibility that the user is unable to resolve drill disconnection error messages.”
- Recall began
- 13 Nov 2023
- Company
- Blue Belt Technologies, Inc
- Device type
- Orthopedic stereotaxic instruments (knee, hip and spine robots) (OLO)
- Concerns
- K231963
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.