HEARTSTART MRX - EMS DEFIBRILLATOR M3536A

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 2015-01-07 for HEARTSTART MRX - EMS DEFIBRILLATOR M3536A manufactured by Philips Medical Systems.

Event Text Entries

[5305752] It was reported to philips that the device would not acquire leads ecg and was showing a "device error. Service required" message with a red x and chip. There was no negative pt impact.
Patient Sequence No: 1, Text Type: D, B5


[12642797] Pr#: (b)(4). A follow up report will be submitted upon completion of the investigation.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1218950-2015-00073
MDR Report Key4407204
Report Source06
Date Received2015-01-07
Date of Report2014-12-09
Date Mfgr Received2014-12-09
Device Manufacturer Date2011-06-01
Date Added to Maude2015-01-26
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationPARAMEDIC
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactGREG THEOKAS
Manufacturer Street3000 MINUTEMAN RD.
Manufacturer CityANDOVER MA 018101099
Manufacturer CountryUS
Manufacturer Postal018101099
Manufacturer Phone9786871501
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameHEARTSTART MRX - EMS DEFIBRILLATOR
Generic NameDEFIBRILLATOR
Product CodeMJK
Date Received2015-01-07
Returned To Mfg2014-12-15
Model NumberM3536A
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerPHILIPS MEDICAL SYSTEMS
Manufacturer Address3000 MINUTEMAN RD. ANDOVER MA 01810109 US 01810 1099


Patients

Patient NumberTreatmentOutcomeDate
10 2015-01-07

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