FUSE FSC-3300-ST 60093

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2019-02-15 for FUSE FSC-3300-ST 60093 manufactured by Boston Scientific Corporation.

Event Text Entries

[136270073] The exact date of the event is unknown. The provided event date was chosen as a best estimate based on the date that the manufacturer became aware of the event. (b)(4). A fuse 1c colonoscope was received for analysis. A functional evaluation was performed and the center image flickers when angulated due to an internal wiring failure of the charged couple device (ccd). The ccd was replaced to resolve the issue. The reported issue was confirmed. The cause of the reported failure is due to ccd failure. Therefore, the assigned investigation conclusion code for this complaint is designated as cause traced to component failure. The repair history was reviewed and nothing was found to indicate a possible service-related cause for the complaint.
Patient Sequence No: 1, Text Type: N, H10


[136270074] It was reported to boston scientific corporation that a fuse 1c colonoscope was used during a colonoscopy procedure performed on a unknown date. According to the complainant, during the procedure, the center image flickered, turned pink then went black. The patient's anatomy was not visible on the center image when the center camera went black. Another fuse 1c colonoscope was used to complete the procedure. There were no patient complications reported as a result of this event.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3005099803-2019-00720
MDR Report Key8343462
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2019-02-15
Date of Report2019-02-15
Date of Event2019-01-01
Date Mfgr Received2019-01-23
Device Manufacturer Date2014-08-22
Date Added to Maude2019-02-15
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 ContactCAROLE MORLEY
Manufacturer Street300 BOSTON SCIENTIFIC WAY
Manufacturer CityMARLBOROUGH MA 01752
Manufacturer CountryUS
Manufacturer Postal01752
Manufacturer Phone5086834015
Manufacturer G1ENDOCHOICE, INC.
Manufacturer Street11810 WILLS ROAD ,
Manufacturer CityALPHARETTA GA 30009
Manufacturer CountryUS
Manufacturer Postal Code30009
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameFUSE
Generic NameENDOSCOPE, ACCESSORIES, IMAGE POST-PROCESSING FOR COLOR ENHANCEMENT
Product CodePEA
Date Received2019-02-15
Returned To Mfg2019-01-23
Model NumberFSC-3300-ST
Catalog Number60093
Lot NumberF1C0807E1C
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerBOSTON SCIENTIFIC CORPORATION
Manufacturer Address300 BOSTON SCIENTIFIC WAY MARLBOROUGH MA 01752 US 01752


Patients

Patient NumberTreatmentOutcomeDate
10 2019-02-15

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