FDA Adverse Event
Death
Summary report: N
VIRIDIA INFORMATION CENTER
MDR report key: 280413
·
Received May 30, 2000
Report
- Report Number
- 1218950-2000-00021
- Event Type
- Death
- Date Received
- May 30, 2000
- Report Date
- May 1, 2000
- Manufacturer
- AGILENT TECHNOLOGIES, INC.
- Product Code
- DRT
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NV, US
- Reporter Occupation
- UNKNOWN
Narratives
Description of Event or Problem · 1
IT WAS REPORTED TO AGILENT TECHNOLOGIES THAT THE EQUIPMENT ALARMS TOO OFTEN FOR THINGS THAT IT SHOULDN'T ALARM FOR. ON THIS PARTICULAR PT, FACILITY HAD NOT PAID ATTENTION TO THE ALARMS BECAUSE OF REPEATED NON-CRITICAL ALARMS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | VIRIDIA INFORMATION CENTER | ARRHYTHMIA | DRT | AGILENT TECHNOLOGIES, INC. | M3150A | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNKNOWN | Death |