FDA Adverse Event
Other
Summary report: N
VIRIDIA INFORMATION CENTER
MDR report key: 261137
·
Received February 5, 2000
Report
- Report Number
- 1218950-2000-00009
- Event Type
- Other
- Date Received
- February 5, 2000
- Date of Event
- January 5, 2000
- Report Date
- January 6, 2000
- Manufacturer
- AGILENT TECHNOLOGIES, INC.
- Product Code
- DRT
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- AL, US
- Reporter Occupation
- BIOMEDICAL ENGINEER
Narratives
Description of Event or Problem · 1
PT BEING MONITORED ON VIRIDIA CENTRAL AT NURSES' DESK WITH CLIENT IN MAIN MONITORING ROOM LOCATED IN ANOTHER FACILITY TWO BLOCKS AWAY. NURSE NOTICED PT GOING INTO VENTRICULAR FIBRILLATION, UNIT LIGHTING UP RED IN SECTOR BUT NO AUDIBLE ALARM. PT CONTINUED TO GO BAD AND FINALLY EXPIRED. NURSE CLAIMS NO AUDIBLE ALARM.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | VIRIDIA INFORMATION CENTER | VIRIDIA | DRT | AGILENT TECHNOLOGIES, INC. | M3150A | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NO INFO | Death |