FDA Adverse Event
Malfunction
Summary report: N
8030916-2008-00058
MDR report key: 1327611
·
Received January 28, 2009
Report
- Report Number
- 8030916-2008-00058
- Event Type
- Malfunction
- Date Received
- January 28, 2009
- Product Code
- FNG
- Removal / Correction Number
- PENDING OFFICIAL "Z" REC
- Report Source
- Manufacturer report
Narratives
Additional Manufacturer Narrative · 1
FOLLOW UP REPORT WILL BE FORWARDED ONCE TECHNICAL ANALYSIS IS COMPLETE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | FNG |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |