AFFINITI 70 - 795210 989605416151

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-01-22 for AFFINITI 70 - 795210 989605416151 manufactured by Philips Ultrasound, Inc.

Event Text Entries

[175914673] An investigation is underway to determine the root cause of the issue. Results of the investigation will be included in a follow up report upon its completion.
Patient Sequence No: 1, Text Type: N, H10


[175914694] A customer reported encountering an incident involving their affiniti ultrasound system becoming unresponsive during an emergency exam of a patient with a ruptured thoracic abdominal aortic aneurysm. The patient ultimately expired from the condition. The system failure occurred when alternating from a c5-1 to an s5-1 transducer. The system was promptly restarted to regain functionality. There was no allegation that the system lockup led to the patient? S outcome.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3019216-2020-00004
MDR Report Key9616898
Report SourceHEALTH PROFESSIONAL
Date Received2020-01-22
Date of Report2020-01-15
Date of Event2020-01-05
Date Mfgr Received2020-01-15
Date Added to Maude2020-01-22
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 ContactMR. PAUL CORRIGAN
Manufacturer Street22100 BOTHELL EVERETT HIGHWAY
Manufacturer CityBOTHELL WA 98021
Manufacturer CountryUS
Manufacturer Postal98021
Manufacturer Phone4254877000
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 NameAFFINITI 70 - 795210
Generic NameSYSTEM, IMAGING, PULSED ECHO, ULTRASONIC
Product CodeIYN
Date Received2020-01-22
Model Number989605416151
Lot NumberUS918F0089
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerPHILIPS ULTRASOUND, INC
Manufacturer Address22100 BOTHELL EVERETT HIGHWAY BOTHELL WA 98021 US 98021


Patients

Patient NumberTreatmentOutcomeDate
101. Death 2020-01-22

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