FDA Adverse Event
Injury
Summary report: N
RIATA ST ACTIVE FIXATION LEAD
MDR report key: 1050885
·
Received May 27, 2008
Report
- Report Number
- 2017865-2008-01827
- Event Type
- Injury
- Date Received
- May 27, 2008
- Date of Event
- March 21, 2008
- Manufacturer
- ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION
- Product Code
- LWS
- PMA / PMN Number
- PMA00001
- Removal / Correction Number
- NA
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- AZ
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
Additional Manufacturer Narrative · 1
NO MEDWATCH FORM WAS RECEIVED.
Description of Event or Problem · 1
THE PACE/SENSE PORTION OF THE LEAD WAS CAPPED DUE TO NOISE OBSERVED ON THE EGMS. WHEN THE PACE/SENSE WAS REMOVED, ABRASIONS WERE NOTED ON THE LEAD DISTAL TO THE TRIFURCATION, AND LIQUID WAS NOTED IN THE INSULATION. THE DEFIB PORTION OF THE LEAD REMAIN IN USE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | RIATA ST ACTIVE FIXATION LEAD | NO BNCN FOUND FOR THIS DEVICE | LWS | ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION | 7000/60 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention |