CARDIOCAP 5

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 2011-05-26 for CARDIOCAP 5 manufactured by Ge Healthcare Finland Oy.

Event Text Entries

[17412037] It was reported that a user smelled smoke coming from the back of the unit due to a presumed failure of the power supply. There were no reports of injury. Ge healthcare's investigation into the reported occurrence is ongoing. A f/u report will be submitted when the investigation has been completed.
Patient Sequence No: 1, Text Type: D, B5


[17653494] Initial reporter's occupation not known at this time.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number9610105-2011-00014
MDR Report Key2146020
Report Source06
Date Received2011-05-26
Date of Report2011-05-27
Date of Event2011-02-04
Date Mfgr Received2011-02-04
Device Manufacturer Date2005-12-01
Date Added to Maude2011-10-17
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional0
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactJOY SONSALLA
Manufacturer Street3000 N. GRANDVIEW BLVD. W450
Manufacturer CityWAUKESHA WI 53188
Manufacturer CountryUS
Manufacturer Postal53188
Manufacturer Phone2625482661
Manufacturer G1GE HEALTHCARE FINLAND, OY
Manufacturer CityHELSINKI
Manufacturer CountryFI
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCARDIOCAP 5
Generic NameCONFIGURED MONITORS
Product CodeMLD
Date Received2011-05-26
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerGE HEALTHCARE FINLAND OY
Manufacturer AddressHELSINKI FI


Patients

Patient NumberTreatmentOutcomeDate
10 2011-05-26

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