FDA Adverse Event
Death
Summary report: N
CODEMASTER 100
MDR report key: 334283
·
Received May 21, 2001
Report
- Report Number
- 1218950-2001-00138
- Event Type
- Death
- Date Received
- May 21, 2001
- Date of Event
- April 24, 2001
- Report Date
- April 24, 2001
- Manufacturer
- AGILENT TECHNOLOGIES, INC.
- Product Code
- LDD
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NE, US
- Reporter Occupation
- PARAMEDIC
Narratives
Description of Event or Problem · 1
IT WAS REPORTED TO AGILENT TECHNOLOGIES THAT THE UNIT DID NOT PACE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 23709 | CODEMASTER 100 | PORTABLE DEFIB/MON | LDD | AGILENT TECHNOLOGIES, INC. | M2475B | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 76 YR | Death |