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 2012-03-23 for CARDIOCAP 5 manufactured by Ge Healthcare.

Event Text Entries

[2575373] It was reported that the cardiocap 5 monitor was not syncing correctly with the lithotripsy unit. There was no serious injury or death associated with this event, nor was medical intervention required. Ge healthcare's investigation is ongoing. A f/u report will be submitted once the investigation has been completed.
Patient Sequence No: 1, Text Type: D, B5


[9840177] The device manufacture date is unk.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number9610105-2012-00016
MDR Report Key2507780
Report Source06
Date Received2012-03-23
Date of Report2012-02-23
Date of Event2012-02-23
Date Mfgr Received2012-02-23
Date Added to Maude2012-09-04
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 W. GRANDVIEW BLVD. W450
Manufacturer CityWAUKEESHA WI 53188
Manufacturer CountryUS
Manufacturer Postal53188
Manufacturer Phone2625482661
Manufacturer G1GE HEALTHCARE
Manufacturer CityHELSINKI
Manufacturer CountryFI
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCARDIOCAP 5
Generic NamePATIENT MONITOR
Product CodeMLD
Date Received2012-03-23
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerGE HEALTHCARE
Manufacturer AddressHELSINKI FI


Patients

Patient NumberTreatmentOutcomeDate
10 2012-03-23

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