FDA Adverse Event
Death
Summary report: N
TELEMETRY MONITORING SYSTEM
MDR report key: 269581
·
Received March 14, 2000
Report
- Report Number
- 1218950-2000-00010
- Event Type
- Death
- Date Received
- March 14, 2000
- Date of Event
- February 12, 2000
- Report Date
- February 12, 2000
- Manufacturer
- AGILENT TECHNOLOGIES, INC.
- Product Code
- DRT
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- GM
- Reporter Occupation
- MEDICAL TECHNOLOGIST
Narratives
Description of Event or Problem · 1
IT WAS REPORTED TO AGILENT TECHNOLOGIES THAT THE PT HAD EXTREME BRADYCARDIA (HEARTRATE LESS 30 BEATS PER MINUTE. THE PHYSICIAN DID NOT RECOGNIZE AN AUDIBLE VISIBLE ALARM AT THE CENTRAL STATION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | TELEMETRY MONITORING SYSTEM | TELEMETRY | DRT | AGILENT TECHNOLOGIES, INC. | M1400A | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 72 YR | Death |