FDA Adverse Event
Malfunction
Summary report: N
DASH 4000
MDR report key: 1082176
·
Received July 22, 2008
Report
- Report Number
- 1082176
- Event Type
- Malfunction
- Date Received
- July 22, 2008
- Date of Event
- July 14, 2008
- Report Date
- July 22, 2008
- Manufacturer
- GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES
- Product Code
- MHX
- Product Problem
- Yes
- Report Source
- User Facility report
- Reporter Location
- MA, US
- Reporter Occupation
- NURSE
Narratives
Description of Event or Problem · 1
ENTIRE ROOM OF DASH 4000 MONITORS SIMULTANEOUSLY ALARMED NIBP FAILURE. ALL PATIENTS CHECKED AND WERE FINE. MONITORS WERE ALL RESET AND PROBLEM DID NOT RECUR. I WAS TOLD THAT THE MONITORS IN OUR NEWLY OPENED CARDIOVASCULAR CENTER ALARMED THE SAME FAILURE AT THE SAME TIME.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | DASH 4000 | MONITOR, PHYSIOLOGICAL | MHX | GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES | DASH 4000 | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * |