FDA Adverse Event
Malfunction
Summary report: N
6000023-1999-00072
MDR report key: 265914
·
Received November 12, 1999
Report
- Report Number
- 6000023-1999-00072
- Event Type
- Malfunction
- Date Received
- November 12, 1999
- Date of Event
- November 13, 1998
- Removal / Correction Number
- NI
- Report Source
- Manufacturer report
- Reporter Location
- CA
- Reporter Occupation
- PHYSICIAN
Narratives
Description of Event or Problem · 1
PREMATURE BATTERY DEPLETION WAS REPORTED; DEVICE TESTED OUT OF SPECIFICATION AT MFGR'S ANALYSIS.
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * | Other |