FOGARTY OCCLUSION CATHETER 62080822F

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,o report with the FDA on 2020-01-02 for FOGARTY OCCLUSION CATHETER 62080822F manufactured by Edwards Lifesciences, Pr.

MAUDE Entry Details

Report Number2015691-2020-04958
MDR Report Key9540282
Report SourceFOREIGN,HEALTH PROFESSIONAL,O
Date Received2020-01-02
Date of Report2019-10-08
Date of Event2019-06-26
Date Mfgr Received2019-12-16
Device Manufacturer Date2018-12-06
Date Added to Maude2020-01-02
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationPHARMACIST
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. JESSICA ATALLAH
Manufacturer StreetONE EDWARDS WAY
Manufacturer CityIRVINE CA 92614
Manufacturer CountryUS
Manufacturer Postal92614
Manufacturer Phone9492500294
Manufacturer G1EDWARDS LIFESCIENCES, PR
Manufacturer StreetSTATE RD INDUS PK 402 KM 1.4
Manufacturer CityANASCO PR 00610
Manufacturer CountryUS
Manufacturer Postal Code00610
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameFOGARTY OCCLUSION CATHETER
Generic NameCATHETER, INTRAVASCULAR OCCLUDING, TEMPORARY
Product CodeMJN
Date Received2020-01-02
Returned To Mfg2019-12-12
Model Number62080822F
Catalog Number62080822F
Lot Number61708855
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerEDWARDS LIFESCIENCES, PR
Manufacturer AddressSTATE RD INDUS PK 402 KM 1.4 ANASCO PR 00610 US 00610


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-02

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