MEDTRONIC VRV-100 1140333-1

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06,07 report with the FDA on 2000-04-03 for MEDTRONIC VRV-100 1140333-1 manufactured by Medtronic Cardiopulmonary-anaheim.

Event Text Entries

[18156384] The hosp reported that the vacuum relief valve leaked during use. The vacuum relief valve was changed out with no affect to the pt.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2022036-2000-00010
MDR Report Key272946
Report Source05,06,07
Date Received2000-04-03
Date of Report2000-03-31
Date of Event2000-03-01
Date Facility Aware2000-03-01
Report Date2000-03-31
Date Mfgr Received2000-03-02
Date Added to Maude2000-04-12
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
Manufacturer Street4633 E LAPALMA AVE
Manufacturer CityANAHEIM CA 92807
Manufacturer CountryUS
Manufacturer Postal92807
Manufacturer Phone7147793651
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Remedial ActionOT
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameMEDTRONIC VRV-100
Generic NameVACUUM RELIEF VALVE
Product CodeMNJ
Date Received2000-04-03
Model Number1140333-1
Catalog Number1140333-1
Lot NumberUNK
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeUNKNOWN
Device Eval'ed by MfgrR
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key264227
ManufacturerMEDTRONIC CARDIOPULMONARY-ANAHEIM
Manufacturer Address4633 EAST LAPALMA AVE. ANAHEIM CA 92807 US
Baseline Brand NameMEDTRONIC VRV-100
Baseline Generic NameVACUUM RELIEF VALVE
Baseline Model No1140333-1
Baseline Catalog No1140333-1
Baseline IDNA


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2000-04-03

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