FDA Adverse Event
Injury
Summary report: N
CONTAK RENEWAL 3 RF
MDR report key: 1043491
·
Received May 8, 2008
Report
- Report Number
- 2124215-2008-33152
- Event Type
- Injury
- Date Received
- May 8, 2008
- Date of Event
- February 5, 2008
- Report Date
- February 5, 2008
- Manufacturer
- CARDIAC PACEMAKERS, INC
- Product Code
- NIK
- Removal / Correction Number
- NA
- 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 | CONTAK RENEWAL 3 RF | IMPLANTABLE CHF GENERATOR | NIK | CARDIAC PACEMAKERS, INC | H210 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 60 YR | Required Intervention | THE DEVICE 0154/352716 WAS IMPLANTED 15-APR-2002| THE DEVICE 6482 022739 WAS USED DURING THE EVENT.| THE DEVICE 04 / WAS IMPLANTED| THE DEVICE 4086/101612 WAS IMPLANTED 15-APR-2002| THE DEVICE 4555/160580 WAS IMPLANTED 05-NOV-2007 |