FDA Adverse Event
Malfunction
Summary report: N
TENDRIL SDX
MDR report key: 4193542
·
Received January 13, 2014
Report
- Report Number
- 2017865-2014-05525
- Event Type
- Malfunction
- Date Received
- January 13, 2014
- Date of Event
- June 14, 2011
- Manufacturer
- ST. JUDE MEDICAL, INC., CRMD
- Product Code
- DTB
- PMA / PMN Number
- NA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FL, US
- Reporter Occupation
- PHYSICIAN
Narratives
Additional Manufacturer Narrative · 1
THIS HISTORICAL COMPLAINT IS BEING FILED AS PART OF A RETROSPECTIVE REVIEW OF COMPLAINT FILES IN RESPONSE TO A RECENT FDA INSPECTION. THERE IS NO CHANGE TO THE ACTUAL PERFORMANCE OF THE PRODUCT AND THIS REPORT ONLY REPRESENTS AN ENHANCEMENT TO THE REPORTING CRITERIA GOING FORWARD. EVAL DESCRIPTION: THE REPORTED FIELD EVENT OF HELIX DAMAGED WITH RETRACTION WAS NOT CONFIRMED. ANALYSIS WAS NORMAL. NO ANOMALY WAS FOUND.
Description of Event or Problem · 1
IT WAS REPORTED THAT THE LEAD WAS ATTEMPTING TO BE IMPLANTED, HOWEVER WAS ABANDONED DUE TO SEVERAL LEAD DISLODGEMENT DURING IMPLANT. LEAD EXHIBITED HELIX EXTENSION RETRACTION ISSUES AND POSSIBLE DAMAGE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 34691 | TENDRIL SDX | PERMANENT PACEMAKER ELECTRODE | DTB | ST. JUDE MEDICAL, INC., CRMD | 1688TC/52 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 62 YR |