ADVANTX-E LC+

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,05,06 report with the FDA on 2013-02-06 for ADVANTX-E LC+ manufactured by Ge Medical Systems Scs.

Event Text Entries

[3141329] It was reported that images on the exam room live monitor were flickering. The user stated that when the monitor was flickering the images were unusable. This issue may result in a degraded image quality that can prevent completion of an exam. No patient injury or death reported.
Patient Sequence No: 1, Text Type: D, B5


[10514377] Ge healthcare? S investigation is ongoing. A follow up report will be submitted once the investigation has been completed. This malfunction was determined to be reportable as this same malfunction has previously contributed to a serious injury within the last two years. (b)(4).
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number9611343-2013-00001
MDR Report Key2958200
Report Source01,05,06
Date Received2013-02-06
Date of Report2013-01-08
Date of Event2013-01-08
Date Mfgr Received2013-01-08
Device Manufacturer Date1999-02-01
Date Added to Maude2013-04-19
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactJOY SONSALLA
Manufacturer Street3000 N. GRANDVIEW BLVD.
Manufacturer CityWAUKESHA WI 53188
Manufacturer CountryUS
Manufacturer Postal53188
Manufacturer Phone2625482661
Manufacturer G1GE MEDICAL SYSTEMS SCS
Manufacturer Street283 RUE DE LA MINIERE BP 34
Manufacturer CityBUC CEDEX
Manufacturer CountryFR
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameADVANTX-E LC+
Generic NameANGIOGRAPHIC X-RAY SYSTEM
Product CodeIZO
Date Received2013-02-06
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerGE MEDICAL SYSTEMS SCS
Manufacturer Address283 RUE DE LA MINIERE BP 34 BUC CEDEX FR


Patients

Patient NumberTreatmentOutcomeDate
10 2013-02-06

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