MEDTRONIC VENOUS RESERVOIR - 1600ML MVR1600

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 2019-11-14 for MEDTRONIC VENOUS RESERVOIR - 1600ML MVR1600 manufactured by Medtronic Mexico.

MAUDE Entry Details

Report Number9612164-2019-04742
MDR Report Key9320257
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-11-14
Date of Report2019-11-14
Date of Event2019-10-15
Date Mfgr Received2019-10-15
Date Added to Maude2019-11-14
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 ContactPAULA BIXBY
Manufacturer Street8200 CORAL SEA STREET NE
Manufacturer CityMOUNDS VIEW MN 55112
Manufacturer CountryUS
Manufacturer Postal55112
Manufacturer Phone7635055378
Manufacturer G1MEDTRONIC MEXICO
Manufacturer StreetAV. PASEO DEL CUCAPAH #10510
Manufacturer CityTIJUANA,BC 22570
Manufacturer CountryMX
Manufacturer Postal Code22570
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMEDTRONIC VENOUS RESERVOIR - 1600ML
Generic NameRESERVOIR, BLOOD, CARDIOPULMONARY BYPASS
Product CodeDTN
Date Received2019-11-14
Returned To Mfg2019-11-08
Model NumberMVR1600
Catalog NumberMVR1600
Lot NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerMEDTRONIC MEXICO
Manufacturer AddressAV. PASEO DEL CUCAPAH #10510 TIJUANA,BC 22570 MX 22570


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2019-11-14

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