FDA Recall Open, Classified

CORI REAL INTELLIGENCE Robotic Drill, Product No. ROB10013 and ROB10013S

Recall: Z-0708-2024 · Initiated November 13, 2023

Recall

Recall Number
Z-0708-2024
Event Number
93620
Firm
Blue Belt Technologies, Inc
FEI Number
3016090213
Product Code
OLO
Status
Open, Classified
Root Cause
Device Design
Initiated
November 13, 2023
Posted
January 11, 2024
Address
2875 Railroad St, Pittsburgh, PA, 15201

Description

CORI REAL INTELLIGENCE Robotic Drill, Product No. ROB10013 and ROB10013S

Reason

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

Action

The recalling firm sent an Urgent Medical Device Recall/Correction notice, dated 11/13/23, by mail to consignees. The notice informed consignees that they may continue to use affected devices as is provided that they ensure the backup Robotics Instrument Tray is available during surgery and to review the CORI Surgical System User Manual, which provides instructions for solving error messages. If consignees are unable to resolve the error messages, they should be prepared to convert to manual surgical procedure following the instructions in Appendix D: Recovery Procedure Guidelines of the CORI Surgical System User Manual. In accordance with routine servicing, consignees should return the CORI drill after 75 uses for servicing, during which the recalling firm will make the hardware update required to correct this recall event. Consignees are asked to contact their Account Representative to report pervasive drill disconnection error messages. Completed acknowledgement forms are to be returned to the recalling firm by email at [email protected]. Questions are to be directed by email to [email protected] or to your Account Representative.

Distribution

Domestic: Nationwide Distribution.

Quantity

1859 units