EPIQ 7W - 795202

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 2020-03-04 for EPIQ 7W - 795202 manufactured by Philips Ultrasound, Inc.

Event Text Entries

[186850190] A thorough investigation performed by development engineering identified the reported issue as a software anomaly caused by a race condition in the capture code between thumbnail and still frame capture operations. A solution for this issue has been included in a newly released software revision. The site? S local philips service team has been notified through normal service channels. Data from the customer has been collected and analyzed.
Patient Sequence No: 1, Text Type: N, H10


[186850191] A customer reported encountering an incident where a patient? S data was mixed with another exam. According to the feedback details, images from a previous study appeared in the next patient? S exam. The data mix-up was identified by the user and there was no allegation of altered patient outcome as a result of the issue.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3019216-2020-00015
MDR Report Key9789240
Report SourceHEALTH PROFESSIONAL
Date Received2020-03-04
Date of Report2020-02-07
Date Mfgr Received2020-02-07
Date Added to Maude2020-03-04
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 NameEPIQ 7W - 795202
Generic NameSYSTEM, IMAGING, PULSED DOPPLER, ULTRASONIC22
Product CodeIYN
Date Received2020-03-04
Model NumberEPIQ 7W - 795202
Catalog NumberEPIQ 7W - 795202
Lot NumberUSO14B0120
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerPHILIPS ULTRASOUND, INC
Manufacturer Address22100 BOTHELL EVERETT HIGHWAY BOTHELL WA 98021 US 98021


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-04

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