FDA Adverse Event
Malfunction
Summary report: N
TENDRIL STS
MDR report key: 2013913
·
Received March 10, 2011
Report
- Report Number
- 2017865-2011-01688
- Event Type
- Malfunction
- Date Received
- March 10, 2011
- Date of Event
- December 22, 2010
- Manufacturer
- ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION
- Product Code
- DTB
- PMA / PMN Number
- NA
- Removal / Correction Number
- NA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA
- 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 ONE DAY POST IMPLANT, THE RIGHT VENTRICULAR LEAD EXHIBITED BIPOLAR IMPEDANCE OF 2600 OHMS AND HIGH CAPTURE THRESHOLD AT 3.5 V. IN UNIPOLAR, IMPEDANCE WAS 430 OHMS AND THRESHOLDS IMPROVED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | TENDRIL STS | PERMANENT PACEMAKER ELECTRODE | DTB | ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION | 2088TC/52 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 87 YR |