FDA Adverse Event
Malfunction
Summary report: N
RIATA PASSIVE FIXATION
MDR report key: 2962774
·
Received February 14, 2013
Report
- Report Number
- 2938836-2013-00079
- Event Type
- Malfunction
- Date Received
- February 14, 2013
- Date of Event
- January 18, 2013
- Manufacturer
- ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION
- Product Code
- NVY
- PMA / PMN Number
- P950022
- Removal / Correction Number
- Z0457
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
Additional Manufacturer Narrative · 1
ALL INFORMATION PROVIDED BY MANUFACTURER, NO MEDWATCH FORM WAS RECEIVED.
Description of Event or Problem · 1
IT WAS REPORTED THAT AT TIME OF DEVICE CHANGE-OUT, EXTERNALIZED CONDUCTORS WERE NOTED VIA X-RAY. ALL ELECTRICAL MEASUREMENTS WERE NORMAL. PHYSICIAN DECIDED TO LEAVE THE LEAD IMPLANTED AND MONITOR THE LEAD. THE PATIENT'S CONDITION AFTER THE EVENT WAS GOOD.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 64444 | RIATA PASSIVE FIXATION | DEFIBRILLATION LEAD | NVY | ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION | 1570/65 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 79 YR |