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.
[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
Report Number | 1625425-1997-90003 |
MDR Report Key | 81234 |
Report Source | 06,07 |
Date Received | 1997-03-25 |
Date of Event | 1997-02-15 |
Date Mfgr Received | 1997-02-26 |
Date Added to Maude | 1997-04-08 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 0 |
Reporter Occupation | RISK MANAGER |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ARGON PVC EXTENSION TUBE & STOPCOCK |
Generic Name | PVC EXTENSION TUBE & STOPCOCK |
Product Code | FLN |
Date Received | 1997-03-25 |
Model Number | * |
Catalog Number | 041115002A |
Lot Number | UNK |
ID Number | * |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | * |
Device Eval'ed by Mfgr | Y |
Implant Flag | N |
Date Removed | * |
Device Sequence No | 1 |
Device Event Key | 80673 |
Manufacturer | ARGON MEDICAL |
Manufacturer Address | 1444 FLAT CREEK RD ATHENS TX 75751 US |
Baseline Brand Name | ARGON PVC EXTENSION TUBE & STOPCOCK |
Baseline Generic Name | PVC EXTENSION TUBE & STOPCOCK |
Baseline Model No | * |
Baseline Catalog No | 041115002A |
Baseline ID | * |
Baseline Device Family | PATIENT MONITORING |
Baseline Shelf Life [Months] | NA |
Baseline PMA Flag | N |
Baseline 510K PMN | N |
Baseline Preamendment | Y |
Baseline Transitional | N |
510k Exempt | N |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 1997-03-25 |