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Open, Classified

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

FDA Recall Z-0708-2024 · Posted 2024-01-11

Recall StatusOpen, Classified
Product CodeOLO
Date Initiated2023-11-13
Product Quantity1859 units

Reason for Recall

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

Firm 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.

Root Cause

Device Design

Distribution Pattern

Domestic: Nationwide Distribution.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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