FDA Adverse Event
Injury
Summary report: N
VITALITY 2 DR
MDR report key: 1042650
·
Received May 8, 2008
Report
- Report Number
- 2124215-2008-33989
- Event Type
- Injury
- Date Received
- May 8, 2008
- Date of Event
- February 28, 2008
- Report Date
- February 28, 2008
- Manufacturer
- CARDIAC PACEMAKERS, INC
- Product Code
- LWS
- Removal / Correction Number
- Z47/55-07
- 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 2 DR | IMPLANTABLE CARDIOVERTER DEFIBRILLATOR | LWS | CARDIAC PACEMAKERS, INC | T165 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 65 YR | Required Intervention | THE DEVICE 1850/105272 WAS IMPLANTED 09-JAN-2001| THE DEVICE 0145/338701 WAS IMPLANTED 09-JAN-2001| THE DEVICE 4470/460815 WAS IMPLANTED 03-NOV-2005| THE DEVICE 6481 010207 WAS USED DURING THE EVENT. |