FDA Adverse Event
Malfunction
Summary report: N
VITALITY 2 DR EL
MDR report key: 1041974
·
Received May 8, 2008
Report
- Report Number
- 2124215-2008-34657
- Event Type
- Malfunction
- Date Received
- May 8, 2008
- Date of Event
- March 20, 2008
- Report Date
- March 20, 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 EL | IMPLANTABLE CARDIOVERTER DEFIBRILLATOR | LWS | CARDIAC PACEMAKERS, INC | T167 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 65 YR | Other | THE DEVICE 4470/474894 WAS IMPLANTED 29-JUL-2005| THE DEVICE 0185/125993 WAS IMPLANTED 29-JUL-2005 |