FDA Adverse Event
Malfunction
Summary report: N
RIATA ACTIVE FIXATION
MDR report key: 4153669
·
Received October 8, 2014
Report
- Report Number
- 2938836-2014-16489
- Event Type
- Malfunction
- Date Received
- October 8, 2014
- Date of Event
- August 7, 2014
- Manufacturer
- ST. JUDE MEDICAL, INC., CRMD
- Product Code
- NVY
- PMA / PMN Number
- P950022
- Removal / Correction Number
- Z0457
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- AZ, US
- Reporter Occupation
- PHYSICIAN
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 THE ASYMPTOMATIC PATIENT PRESENTED IN THE OPERATING ROOM FOR DEVICE UPGRADE. FLUOROSCOPY REVEALED EXTERNALIZED CONDUCTORS ON THE ACTIVE DEFIB PORTION OF THE LEAD. THE PACE/SENSE PORTION OF THE LEAD WAS CAPPED IN 2011. THE PATIENTS CONDITION WAS FINE AND WILL BE MONITORED WITH ROUTINE FOLLOW-UPS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 631846 | RIATA ACTIVE FIXATION | DEFIBRILLATION LEAD | NVY | ST. JUDE MEDICAL, INC., CRMD | 1580/65 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 67 YR |