FDA Adverse Event
Malfunction
Summary report: N
TENDRIL STS
MDR report key: 3925997
·
Received July 10, 2014
Report
- Report Number
- 2017865-2014-15358
- Event Type
- Malfunction
- Date Received
- July 10, 2014
- Date of Event
- April 18, 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 Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
ALL INFORMATION PROVIDED BY MANUFACTURER, NO MEDWATCH FORM WAS RECEIVED. EVALUATION DESCRIPTION: FAILURE EVENT OBSERVED DURING ANALYSIS. FINAL ANALYSIS FOUND INSULATION DAMAGE AT 26. CM TO 26.9 CM FROM CONNECTOR PIN. OUTER COIL DAMAGE WAS NOTED AT 26.0 CM TO 26.3 CM FROM THE CONNECTOR PIN. THE DAMAGE WAS CONSISTENT WITH THAT OCCURRING DUE TO CLAVICLE CRUSH. (B)(6).
Description of Event or Problem · 1
THIS REPORT IS TO ADVISE OF AN EVENT OBSERVED DURING ANALYSIS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 403428 | TENDRIL STS | PERMANENT PACEMAKER ELECTRODE | NVN | ST. JUDE MEDICAL, INC., CRMD | 2088TC/52 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |