MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,07 report with the FDA on 2003-11-17 for MAC ELECTROCARDIOGRAPH MAC 1200 NA manufactured by Ge Medical Systems Information Technologies.
[350019]
Customer reports their technician entered patient information. They received ecg with previous patient's tracing but current patient's name. The patient was treated with medication.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2124823-2003-00065 |
MDR Report Key | 496199 |
Report Source | 05,07 |
Date Received | 2003-11-17 |
Date of Report | 2003-11-14 |
Date of Event | 2003-10-14 |
Date Mfgr Received | 2003-10-16 |
Date Added to Maude | 2003-11-20 |
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 | 3 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 0 |
Manufacturer Contact | PAUL HANNEMAN |
Manufacturer Street | 8200 W. TOWER AVE. |
Manufacturer City | MILWAUKEE WI 53223 |
Manufacturer Country | US |
Manufacturer Postal | 53223 |
Manufacturer Phone | 4143622404 |
Manufacturer G1 | * |
Manufacturer Street | * |
Manufacturer City | * |
Manufacturer Country | * |
Single Use | 3 |
Previous Use Code | 3 |
Removal Correction Number | NA |
Event Type | 3 |
Type of Report | 3 |
Brand Name | MAC ELECTROCARDIOGRAPH |
Generic Name | ECG ANALYSIS SYSTEM |
Product Code | LOS |
Date Received | 2003-11-17 |
Model Number | MAC 1200 |
Catalog Number | NA |
Lot Number | NA |
ID Number | NA |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Eval'ed by Mfgr | R |
Implant Flag | N |
Date Removed | A |
Device Sequence No | 1 |
Device Event Key | 484932 |
Manufacturer | GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES |
Manufacturer Address | 8200 WEST TOWER AVE. MILWAUKEE WI 53223 US |
Baseline Brand Name | MAC ELECTROCARDIOGRAPH |
Baseline Generic Name | ECG ANALYSIS SYSTEM |
Baseline Model No | MAC 1200 |
Baseline Catalog No | NA |
Baseline ID | NA |
Baseline Device Family | MAC ELECTROCARDIOGRAPH |
Baseline Shelf Life [Months] | NA |
Baseline PMA Flag | N |
Baseline 510K PMN | Y |
Premarket Notification | K991735 |
Baseline Preamendment | N |
Baseline Transitional | N |
510k Exempt | N |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Life Threatening | 2003-11-17 |