VRV-II (NONE-STERILE) 4003203 *

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 1998-02-19 for VRV-II (NONE-STERILE) 4003203 * manufactured by Quest Medical, Inc..

Event Text Entries

[88656] The customer reported that the valve appeared to be occluded. No injury was reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1627487-1998-00003
MDR Report Key151378
Report Source05
Date Received1998-02-19
Date of Report1998-02-19
Date Mfgr Received1998-01-22
Date Added to Maude1998-02-26
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
Single Use3
Remedial ActionRC
Previous Use Code3
Removal Correction NumberZ-162/3-8
Event Type3
Type of Report3

Device Details

Brand NameVRV-II (NONE-STERILE)
Generic NameVACUUM RELIEF VALVE
Product CodeMNJ
Date Received1998-02-19
Model Number4003203
Catalog Number*
Lot NumberUNK
ID Number*
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Implant FlagN
Date Removed*
Device Sequence No1
Device Event Key147525
ManufacturerQUEST MEDICAL, INC.
Manufacturer AddressONE ALLENTOWN PKWY. ALLEN TX 750024211 US
Baseline Brand NameVACUUM RELIEF VALVE-II
Baseline Generic NameONE-WAY VALVE
Baseline Model No4003203
Baseline Catalog NoNA
Baseline IDNA
Baseline Device FamilyCARDIOVASCULAR
Baseline Shelf Life ContainedY
Baseline Shelf Life [Months]*
Baseline PMA FlagN
Baseline 510K PMNY
Premarket NotificationK760894
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
10 1998-02-19

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