FDA Adverse Event
Summary report: N
UNK
MDR report key: 808789
·
Received January 11, 2007
Report
- Report Number
- 808789
- Date Received
- January 11, 2007
- Date of Event
- October 12, 2006
- Report Date
- January 10, 2007
- Manufacturer
- UNK
- Product Code
- HNW
- Report Source
- User Facility report
- Reporter Location
- TX, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
JONES TUBE REMOVAL.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | UNK | UNK | HNW | UNK | UNK | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 65 YR |