Class II

Medical Device Recall: CORI REAL INTELLIGENCE Robotic Drill, Product No. ROB10013 and ROB10013S

Blue Belt Technologies, Inc · November 13, 2023

Reason for Recall

Possibility that the user is unable to resolve drill disconnection error messages.

Distribution

Domestic: Nationwide Distribution.

States Affected

NATIONWIDE

Quantity Affected

1859 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0708-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Blue Belt Technologies, Inc Medical Device Recall: CORI REAL INTELLIGENCE Robotic Drill, Product No. ROB10013 and ROB10013S | SafeCheck