FDA Adverse Event
Other
Summary report: N
MANUFACTURER = PHILIPS MEDICAL SYSTEMS
MDR report key: 747007
·
Received September 29, 2005
Report
- Report Number
- MW1259273
- Event Type
- Other
- Date Received
- September 29, 2005
- Report Date
- September 29, 2005
- Manufacturer
- *
- Product Code
- DRT
- Report Source
- Voluntary report
- Reporter Location
- CA
- Reporter Occupation
- RISK MANAGER
Narratives
Description of Event or Problem · 1
AS THE RESULT OF AN ADVERSE EVENT INOUR FACILITY IN WHICH THERE WAS A DELAY IN RESPONDING TO ALRMS LEADERSHIP DECIDED TO IMPLEMENT ACTION PLAN IN WHICH THE CENTRAL MONITORING SYSTEM CAN NOT BE SILIENCED AT THE NURSE'S STATION, INSTEAD OF ALARMS WOULD NEED TO BE SILENCED AT THE BEDSIDE. HOWEVER UPON PROGRAMMING THE ALARMS IT WAS DISCOVERED THAT BOHT RED AND YELLOW ALARMS HAVE TO BE RESET AT THE SITE I.E., EITHER THE PT ROOM OR THE CENTRAL STATION. IDEAL PROGRAMMING WOULD ALLOW THE CHOICE FOR YELLOW ALARMS TO BE SILENCED AT THE CENTRAL STATION AND RED ALARMS TO BE SILENCED AT THE BEDSIDE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | MANUFACTURER = PHILIPS MEDICAL SYSTEMS | CENTRAL MONITORING SYSTEM | DRT | * | M3150A | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 33 YR | Other |