AVALON FM30 FETAL MONITOR M2703A 862199

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,user facility report with the FDA on 2019-02-12 for AVALON FM30 FETAL MONITOR M2703A 862199 manufactured by Philips Medical Systems.

Event Text Entries

[135885267] A follow up report will be submitted once the investigation is complete. Serial number not provided at time of report.
Patient Sequence No: 1, Text Type: N, H10


[135885268] The customer reported the death of a newborn after an emergency c-section and 19 minutes of attempted resuscitation. According to the customer (biomedical engineer) and caregivers, artifacts between the mother? S pulse and the fetus' pulse rate were identified. But they think the device worked properly.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9610816-2019-00044
MDR Report Key8331468
Report SourceFOREIGN,USER FACILITY
Date Received2019-02-12
Date of Report2019-02-05
Date of Event2019-02-03
Date Mfgr Received2019-02-05
Device Manufacturer Date2017-04-10
Date Added to Maude2019-02-12
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationBIOMEDICAL ENGINEER
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. BETTY HARRIS
Manufacturer StreetHEWLETT-PACKARD STR.2
Manufacturer CityBOEBLINGEN 71034
Manufacturer CountryGM
Manufacturer Postal71034
Manufacturer G1PHILIPS MEDICAL SYSTEMS
Manufacturer Street3000 MINUTEMAN ROAD
Manufacturer CityANDOVER MA 01810
Manufacturer CountryUS
Manufacturer Postal Code01810
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameAVALON FM30 FETAL MONITOR
Generic NameFETAL MONITOR
Product CodeHGM
Date Received2019-02-12
Model NumberM2703A
Catalog Number862199
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerPHILIPS MEDICAL SYSTEMS
Manufacturer AddressHEWLETT-PACKARD STR.2 BOEBLINGEN 71034 GM 71034


Patients

Patient NumberTreatmentOutcomeDate
101. Death 2019-02-12

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