FDA Adverse Event
Death
Summary report: N
VIRIDIA 24/26 COMPONENT MONITORING SYSTEM
MDR report key: 370064
·
Received January 4, 2002
Report
- Report Number
- 1218950-2002-00001
- Event Type
- Death
- Date Received
- January 4, 2002
- Date of Event
- December 5, 2001
- Report Date
- December 7, 2001
- Manufacturer
- AGILENT TECHNOLOGIES, INC.
- Product Code
- DRT
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- VA, US
- Reporter Occupation
- NURSE
Narratives
Description of Event or Problem · 1
THE CUSTOMER REPORTED THAT THE ALARM DID NOT ANNUNCIATE DURING ALARM CONDITION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | VIRIDIA 24/26 COMPONENT MONITORING SYSTEM | BEDSIDE MONITOR | DRT | AGILENT TECHNOLOGIES, INC. | M1205A | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 55 YR | Death |