POWERHEART G5 KIT, AUTO, DAN/INTL ENG G5A-14A

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign report with the FDA on 2020-03-31 for POWERHEART G5 KIT, AUTO, DAN/INTL ENG G5A-14A manufactured by Cardiac Science Corporation.

Event Text Entries

[186752165] Zoll medical corporation has not received the device for evaluation and this complaint is still under investigation.
Patient Sequence No: 1, Text Type: N, H10


[186752166] Complainant alleged that during functional testing,the device displayed an "ecg fault -501" error message. Complainant did not indicate that there was any patient involvement in the reported malfunction.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2112020-2020-00205
MDR Report Key9903663
Report SourceFOREIGN
Date Received2020-03-31
Date of Report2020-03-10
Date Mfgr Received2020-03-10
Device Manufacturer Date2019-02-06
Date Added to Maude2020-03-31
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 Street269 MILL ROAD
Manufacturer CityCHELMSFORD MA 01824
Manufacturer CountryUS
Manufacturer Postal01824
Manufacturer Phone9784219552
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePOWERHEART G5 KIT, AUTO, DAN/INTL ENG
Generic NameAUTOMATED EXTERNAL DEFIBRILLATOR
Product CodeMKJ
Date Received2020-03-31
Model NumberG5A-14A
Catalog NumberG5A-14A
Lot NumberNA
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCARDIAC SCIENCE CORPORATION
Manufacturer Address500 BURDICK PARKWAY DEERFIELD WI 535319692 US 535319692


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-31

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