FDA Adverse Event
Death
Summary report: N
CODEMASTER 100
MDR report key: 380902
·
Received March 4, 2002
Report
- Report Number
- 1218950-2002-00032
- Event Type
- Death
- Date Received
- March 4, 2002
- Date of Event
- February 18, 2002
- Report Date
- February 18, 2002
- Manufacturer
- AGILENT TECHNOLOGIES, INC.
- Product Code
- LDD
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
THE CUSTOMER REPORTED THAT WHEN THE PATIENT CODED, THE CODEMASTER 100 WOULD NOT WORK. WHEN THE BATTERY WAS REPLACED, THE UNIT WORKED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | CODEMASTER 100 | PORTABLE DEFIB/MON | LDD | AGILENT TECHNOLOGIES, INC. | M2475B | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 68 YR | Death |