FDA Adverse Event
Other
Summary report: N
EMORY RESPOSABLE DISS CVD
MDR report key: 504164
·
Received January 2, 2004
Report
- Report Number
- 1038548-2004-00001
- Event Type
- Other
- Date Received
- January 2, 2004
- Date of Event
- June 17, 2003
- Report Date
- January 2, 2004
- Manufacturer
- SNOWDEN PENCER, INC.
- Product Code
- GEI
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TX, US
- Reporter Occupation
- NURSE
Narratives
Description of Event or Problem · 1
INSULATION BURNED OFF AND INSTRUMENT BURNED PATIENT ON TWO SEPARATE OCCASIONS, ONCE IN 2003, AND ONCE IN ABOUT A MONTH EARLIER.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | EMORY RESPOSABLE DISS CVD | * | GEI | SNOWDEN PENCER, INC. | 88-5227 | 774553 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNKNOWN |