FDA Adverse Event
Injury
Summary report: N
VITALITY AVT
MDR report key: 1043123
·
Received May 8, 2008
Report
- Report Number
- 2124215-2008-33512
- Event Type
- Injury
- Date Received
- May 8, 2008
- Date of Event
- February 14, 2008
- Report Date
- February 14, 2008
- Manufacturer
- CARDIAC PACEMAKERS, INC
- Product Code
- LWS
- Removal / Correction Number
- Z47/53-08
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MN, US
- Reporter Occupation
- LAY USER/PATIENT
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | VITALITY AVT | IMPLANTABLE CARDIOVERTER DEFIBRILLATOR | LWS | CARDIAC PACEMAKERS, INC | A135 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 56 YR | Required Intervention | THE DEVICE 4469/326605 WAS IMPLANTED 30-APR-2003| THE DEVICE 0158/116668 WAS IMPLANTED 30-APR-2003 |