FDA Adverse Event
Injury
Summary report: N
GUIDANT CORP
MDR report key: 789831
·
Received November 16, 2006
Report
- Report Number
- 789831
- Event Type
- Injury
- Date Received
- November 16, 2006
- Date of Event
- April 19, 2006
- Report Date
- November 9, 2006
- Manufacturer
- GUIDANT CORP
- Product Code
- LWS
- Adverse Event
- Yes
- Report Source
- User Facility report
- Reporter Location
- HI, US
- Reporter Occupation
- RISK MANAGER
Narratives
Description of Event or Problem · 1
ICD DISCHARGE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | GUIDANT CORP | ICD GENERATOR | LWS | GUIDANT CORP | H179 | NA | |
| 2 | GUIDANT CORP | ICD GENERATOR | LWS | GUIDANT CORP | 6744 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 78 YR | Required Intervention |