FDA Adverse Event
Malfunction
Summary report: N
VENTAK PRIZM HE VR
MDR report key: 1041777
·
Received May 8, 2008
Report
- Report Number
- 2124215-2008-34879
- Event Type
- Malfunction
- Date Received
- May 8, 2008
- Date of Event
- March 28, 2008
- Report Date
- March 28, 2008
- Manufacturer
- CARDIAC PACEMAKERS, INC
- Product Code
- LWS
- Removal / Correction Number
- NA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- US
- Reporter Occupation
- OTHER
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | VENTAK PRIZM HE VR | IMPLANTABLE CARDIOVERTER DEFIBRILLATOR | LWS | CARDIAC PACEMAKERS, INC | 1852 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 47 YR | Other |