CorPath GRX Extended Reach Arm 312Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00816280023123), received between Sep 4, 2019 and Sep 4, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Electrical Shorting” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 4, 2019Electrical Shorting; Electrical Shorting

  DURING PREPARATION FOR A HOSPITAL TRAINING EVENT, IT WAS OBSERVED THAT THE ROBOTIC DRIVE WAS FUNCTIONING AS IF THERE WAS A LOOSE CONNECTION AND UNEXPECTEDLY SHUT DOWN. UPON INVESTIGATION IT WAS OBSERVED THAT A BURNT PORT WAS PRESENT AN ELECTRICAL CONNECTOR OF THE EXTENDED REACH ARM.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 8961205 ↗