ESOPHYX Z R2007

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2019-09-17 for ESOPHYX Z R2007 manufactured by Endogastric Solutions, Inc..

Event Text Entries

[162692224] The physician is not alleging a device malfunction causing or contributing to the serious adverse event. No issues were reported by the physician or the endogastric solutions representative during the tif procedure or post-procedure egd. No further information has been provided to egs as of the date of this report. A follow-up report will be submitted if more information is obtained.
Patient Sequence No: 1, Text Type: N, H10


[162692225] A patient was admitted to the hospital the day after a successful hiatal hernia repair + tif procedure. The patient was diagnosed with an esophageal perforation and was septic. A drain was placed in an unknown location during treatment.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3005473391-2019-00124
MDR Report Key9079651
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2019-09-17
Date of Report2019-09-17
Date of Event2019-08-20
Date Mfgr Received2019-08-27
Date Added to Maude2019-09-17
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 ContactMR. VISHNU VENKATESAN
Manufacturer Street18109 NE 76TH ST SUITE 100
Manufacturer CityREDMOND WA 98052
Manufacturer CountryUS
Manufacturer Postal98052
Manufacturer Phone4253079248
Manufacturer G1ENDOGASTRIC SOLUTIONS, INC.
Manufacturer Street18109 NE 76TH ST SUITE 100
Manufacturer CityREDMOND WA 98052
Manufacturer CountryUS
Manufacturer Postal Code98052
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameESOPHYX Z
Generic NameODE
Product CodeODE
Date Received2019-09-17
Model NumberR2007
Catalog NumberR2007
Lot NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerENDOGASTRIC SOLUTIONS, INC.
Manufacturer Address18109 NE 76TH ST. SUITE 100 REDMOND WA 98052 US 98052


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Required No Informationntervention 2019-09-17

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