EDWARDS PERICARDIAL PATCH 4700 NA

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,02 report with the FDA on 1999-04-16 for EDWARDS PERICARDIAL PATCH 4700 NA manufactured by Baxter Healthcare Corp..

Event Text Entries

[174161] This pt reportedly expired due to cardiac failure. No further info was provided.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number6000002-1999-00094
MDR Report Key219270
Report Source01,02
Date Received1999-04-16
Date of Report1999-03-19
Date of Event1998-03-07
Date Mfgr Received1999-03-19
Device Manufacturer Date1997-10-01
Date Added to Maude1999-04-20
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameEDWARDS PERICARDIAL PATCH
Generic NamePERICARDIAL PATCH
Product CodeMFX
Date Received1999-04-16
Model Number4700
Catalog NumberNA
Lot NumberF60121A
ID NumberNA
Device Expiration Date2001-10-01
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Age9 MO
Device Eval'ed by MfgrR
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key212648
ManufacturerBAXTER HEALTHCARE CORP.
Manufacturer Address17221 RED HILL AVENUE IRVINE CA 92614 US
Baseline Brand NameEDWARDS PERICARDIAL PATCH
Baseline Generic NameNA
Baseline Model No4700
Baseline Catalog NoNA
Baseline IDNA
Baseline Device FamilyPERICARDIAL PATCH
Baseline Shelf Life ContainedY
Baseline Shelf Life [Months]48
Baseline PMA FlagN
Baseline 510K PMNY
Premarket NotificationK833763
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
101. Death 1999-04-16

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