CARMEDA PEDIATRIC BIO-PROBE CBDP-38P 95140

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,05,06,07 report with the FDA on 2003-02-20 for CARMEDA PEDIATRIC BIO-PROBE CBDP-38P 95140 manufactured by Medtronic Perfusion Systems.

Event Text Entries

[19901545] Pt placed on ecmo in intensive care following surgery. After an unknown length of time, a leak began at the flow-probe. Before the unit could be changed out, the port broke completely. Pt died the following day.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2184009-2003-00009
MDR Report Key444427
Report Source01,05,06,07
Date Received2003-02-20
Date of Report2003-01-23
Date of Event2003-01-21
Date Mfgr Received2003-01-23
Date Added to Maude2003-02-26
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 Location0
Manufacturer ContactLISA WEIK
Manufacturer Street8299 CENTRAL AVENUE, NE
Manufacturer CityMINNEAPOLIS MN 55432
Manufacturer CountryUS
Manufacturer Postal55432
Manufacturer Phone7635146694
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCARMEDA PEDIATRIC BIO-PROBE
Generic NameEXTRAVASCULAR BLOOD FLOW PROBE
Product CodeDPT
Date Received2003-02-20
Model NumberCBDP-38P
Catalog Number95140
Lot NumberUNK
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key433404
ManufacturerMEDTRONIC PERFUSION SYSTEMS
Manufacturer Address7611 NORTHLAND DR. BROOKLYN PARK MN 55428 US
Baseline Brand NameCARMEDA PEDIATRIC BIO-PROBE
Baseline Generic NameEXTRAVASCULAR BLOOD PLOW PROBE
Baseline Model NoCBDP-38P
Baseline Device FamilyFLOW PROBE
Baseline Shelf Life ContainedY
Baseline Shelf Life [Months]24
Baseline PMA FlagN
Baseline 510K PMNY
Premarket NotificationK891687
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
101. Death 2003-02-20

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