ADEPT 1501571

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2019-07-12 for ADEPT 1501571 manufactured by Baxter Healthcare - Castlebar.

MAUDE Entry Details

Report Number1416980-2019-03741
MDR Report Key8784725
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-07-12
Date of Report2019-07-12
Date Mfgr Received2019-06-18
Date Added to Maude2019-07-12
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer Street25212 W. ILLINOIS ROUTE 120
Manufacturer CityROUND LAKE IL 60073
Manufacturer CountryUS
Manufacturer Postal60073
Manufacturer Phone2242702068
Manufacturer G1BAXTER HEALTHCARE - CASTLEBAR
Manufacturer Street28 MONEEN ROAD
Manufacturer CityCASTELBAR
Manufacturer CountryEI
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameADEPT
Generic NameBARRIER, ABSORABLE, ADHESION
Product CodeMCN
Date Received2019-07-12
Model NumberNA
Catalog Number1501571
Lot NumberASKU
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBAXTER HEALTHCARE - CASTLEBAR
Manufacturer Address28 MONEEN ROAD


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-07-12

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