FDA Adverse Event
Death
Summary report: N
M3155B INFO CTR NETWORK DB
MDR report key: 695281
·
Received April 3, 2006
Report
- Report Number
- 1218950-2006-00104
- Event Type
- Death
- Date Received
- April 3, 2006
- Date of Event
- March 7, 2006
- Report Date
- March 7, 2006
- Manufacturer
- PHILIPS MEDICAL SYSTEMS
- Product Code
- DXG
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FL, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
THE CUSTOMER REPORTED THAT THE DEVICE DID NOT PROVIDE AUDIBLE ALARMS FOR A PATIETN EVENT. THE PT EXPIRED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | M3155B INFO CTR NETWORK DB | CENTRAL STATION NETWORK DATABA | DXG | PHILIPS MEDICAL SYSTEMS | 862068 (M3155B) | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNKNOWN | Death |