ARGON PVC EXTENSION TUBE & STOPCOCK * 041115002A

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06,07 report with the FDA on 1997-03-25 for ARGON PVC EXTENSION TUBE & STOPCOCK * 041115002A manufactured by Argon Medical.

Event Text Entries

[20244050] Nurse found hub/luer off tubing of arterial line. Pt lost estimated 5-50cc's of blood.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1625425-1997-90003
MDR Report Key81234
Report Source06,07
Date Received1997-03-25
Date of Event1997-02-15
Date Mfgr Received1997-02-26
Date Added to Maude1997-04-08
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Reporter OccupationRISK MANAGER
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameARGON PVC EXTENSION TUBE & STOPCOCK
Generic NamePVC EXTENSION TUBE & STOPCOCK
Product CodeFLN
Date Received1997-03-25
Model Number*
Catalog Number041115002A
Lot NumberUNK
ID Number*
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Age*
Device Eval'ed by MfgrY
Implant FlagN
Date Removed*
Device Sequence No1
Device Event Key80673
ManufacturerARGON MEDICAL
Manufacturer Address1444 FLAT CREEK RD ATHENS TX 75751 US
Baseline Brand NameARGON PVC EXTENSION TUBE & STOPCOCK
Baseline Generic NamePVC EXTENSION TUBE & STOPCOCK
Baseline Model No*
Baseline Catalog No041115002A
Baseline ID*
Baseline Device FamilyPATIENT MONITORING
Baseline Shelf Life [Months]NA
Baseline PMA FlagN
Baseline 510K PMNN
Baseline PreamendmentY
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 1997-03-25

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