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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: BARCO NV BARCO; NEXXISOR, NMS
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BARCO NV BARCO; NEXXISOR, NMS Back to Search Results
Model Number NEXXISOR NMS
Device Problem No Display/Image (1183)
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Date 03/09/2022
Event Type  malfunction  
Event Description
Reported failure: problem in oslo intervention or7 - hybrid or.All sources had disappeared from the screen.We did a remote login and could not reach nms.Pc and nms service restarted a few times, no luck.All other vlans on the switch unaffected and all other nms fully functional.Nms uninstalled, renamed the programme data and deleted the programme files and then a new install of nms.After re-install, reconfiguration of nms and re-licensing nms was working again.This was very unfortunate as the patient was already on the table and ready to start the operation this morning.The operation had to be delayed by 35 minutes until i had the system repaired.Luckily we got it back working.
 
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Brand Name
BARCO
Type of Device
NEXXISOR, NMS
Manufacturer (Section D)
BARCO NV
president kennedypark 35
kortrijk, west-vlaanderen 8500
BE  8500
Manufacturer Contact
lieven de wandel
president kennedypark 35
kortrijk, west-vlaanderen 8500
BE   8500
MDR Report Key18796475
MDR Text Key336516127
Report Number3004455125-2024-00008
Device Sequence Number1
Product Code DXJ
Combination Product (y/n)N
Reporter Country CodeUK
PMA/PMN Number
K173381
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Foreign
Reporter Occupation Other
Remedial Action Modification/Adjustment
Type of Report Initial
Report Date 02/14/2024
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Model NumberNEXXISOR NMS
Was Device Available for Evaluation? No
Initial Date Manufacturer Received 03/09/2022
Initial Date FDA Received02/28/2024
Was Device Evaluated by Manufacturer? Yes
Is the Device Single Use? No
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Unknown
Patient Sequence Number1
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