CorPath GRX Drape, Robotic Drive and Arm 309Recalls & reported problems
Corindus, Inc. · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00816280023093), received between May 15, 2020 and May 15, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Product Quality Problem” (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 16, 2026.
Most reported problems
Device problems
- Product Quality Problem1
Patient problems
- No Patient Involvement1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 15, 2020Product Quality Problem; Product Quality Problem
STAFF FOUND A TEAR IN THE ROBOTIC ARM AND DRIVE DRAPE WHEN SETTING UP FOR A CORPATH GRX PROCEDURE.
Patient problems: No Patient Involvement
MAUDE report 10062272 ↗
Other System, Catheter Control, Steerable devices
- CorPath GRX Robotic Drive 303Corindus, Inc. · System, Catheter Control, Steerable7 reports
- CorPath GRX Control Console 301Corindus, Inc. · System, Catheter Control, Steerable7 reports
- CorPath GRX Extended Reach Arm 302Corindus, Inc. · System, Catheter Control, Steerable5 reports
- CorPath GRX Cassette 305Corindus, Inc. · System, Catheter Control, Steerable4 reports
- CorPath GRX Extended Reach Arm 312Corindus, Inc. · System, Catheter Control, Steerable1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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