CORPATH GRX SYSTEM 303

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2019-04-17 for CORPATH GRX SYSTEM 303 manufactured by Corindus, Inc..

Event Text Entries

[146649929] Visual inspection during a servicing event showed that electrical shielding from some wires were damaged. A review of manufacturing and installation records indicated that the system was manufactured and installed per specification. As such, it is likely that the user damaged the cable at some point. No patient or user injury was reported as a result of this malfunction. In addition, the operator's manual for the system warns the user against the use of the system with damaged cabling. Specifically the operator's manual states "operator injury could result from worn cabling or disassembly of the unit. To avoid exposure to potentially hazardous voltages, do not disassemble the corpath grx system outside of the instructions in this manual. Word cabling also creates voltage hazards. If you detect any worn or damaged cables, do not use the system".
Patient Sequence No: 1, Text Type: N, H10


[146649930] During a service event, it was discovered that the electrical cables of the robotic drive and extended reach arm were damaged.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3007822508-2019-00001
MDR Report Key8522776
Report SourceCOMPANY REPRESENTATIVE
Date Received2019-04-17
Date of Report2019-04-12
Date of Event2019-04-03
Date Mfgr Received2019-04-03
Date Added to Maude2019-04-17
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. ROBERT LAVADO
Manufacturer Street309 WAVERLEY OAKS ROAD SUITE 105
Manufacturer CityWALTHAM MA 02452
Manufacturer CountryUS
Manufacturer Postal02452
Manufacturer Phone5086533355
Manufacturer G1CORINDUS, INC.
Manufacturer Street309 WAVERLEY OAKS ROAD SUITE 105
Manufacturer CityWALTHAM MA 02452
Manufacturer CountryUS
Manufacturer Postal Code02452
Single Use3
Remedial ActionRP
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCORPATH GRX SYSTEM
Generic NameCORPATH GRX SYSTEM
Product CodeDXX
Date Received2019-04-17
Model Number303
Catalog Number303
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerCORINDUS, INC.
Manufacturer Address309 WAVERLEY OAKS ROAD SUITE 105 WALTHAM MA 02452 US 02452


Patients

Patient NumberTreatmentOutcomeDate
10 2019-04-17

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.