FDA Adverse Event
Malfunction
Summary report: N
TENDRIL ST
MDR report key: 3923376
·
Received July 9, 2014
Report
- Report Number
- 2017865-2014-14659
- Event Type
- Malfunction
- Date Received
- July 9, 2014
- Date of Event
- May 6, 2014
- Manufacturer
- ST. JUDE MEDICAL, INC., CRMD
- Product Code
- NVN
- PMA / PMN Number
- NA
- Removal / Correction Number
- NA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA, US
- Reporter Occupation
- NURSE
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 LOW LEVELS OF NOISE WERE OBSERVED ON THE ASYMPTOMATIC PATIENTS ATRIAL LEAD. THE NOISE COULD BE REPRODUCED THROUGH ISOMETRIC EXERCISES. THE PATIENT DID NOT HAVE AN ACTIVE CARDIOLOGIST AT THE TIME. THE CLINICIAN WOULD PLAN A COURSE OF ACTION ONCE A PHYSICIAN WAS CHOSEN.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 401829 | TENDRIL ST | PERMANENT PACEMAKER ELECTRODE | NVN | ST. JUDE MEDICAL, INC., CRMD | 1882TC/46 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 80 YR |