BIPAP A40 1111169

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 2020-03-20 for BIPAP A40 1111169 manufactured by Philips Respironics Inc..

Event Text Entries

[184260758] The manufacturer received information alleging a patient became unresponsive and no alarm sounded while on a bipap a40. The patient was transferred to the icu and placed on mechanical ventilation and later expired. The device has yet to be returned to the manufacturer for evaluation. A follow up report will be filed when the manufacturer has completed the investigation.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2518422-2020-00661
MDR Report Key9859683
Report SourceFOREIGN,USER FACILITY
Date Received2020-03-20
Date of Report2020-03-17
Date of Event2020-02-28
Date Mfgr Received2020-03-17
Device Manufacturer Date2015-06-16
Date Added to Maude2020-03-20
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 ContactADAM PRICE
Manufacturer Street1001 MURRY RIDGE LANE
Manufacturer CityMURRYSVILLE, PA
Manufacturer CountryUS
Manufacturer G1PHILIPS RESPIRONICS INC.
Manufacturer Street1001 MURRY RIDGE LANE
Manufacturer CityMURRYSVILLE, PA
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBIPAP A40
Generic NameVENTILATOR, CONTINUOUS, MINIMAL VENTILATORY SUPPORT, FACILITY USE
Product CodeMNT
Date Received2020-03-20
Model Number1111169
Catalog Number1111169
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerPHILIPS RESPIRONICS INC.
Manufacturer Address1001 MURRY RIDGE LANE MURRYSVILLE, PA US


Patients

Patient NumberTreatmentOutcomeDate
101. Death 2020-03-20

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