FDA Adverse Event
Malfunction
Summary report: N
ELLIPSE DR, DF-4 CONNECTOR
MDR report key: 4091985
·
Received January 13, 2014
Report
- Report Number
- 2938836-2014-05121
- Event Type
- Malfunction
- Date Received
- January 13, 2014
- Date of Event
- August 31, 2012
- Manufacturer
- ST. JUDE MEDICAL, INC. CRMD
- Product Code
- LWS
- PMA / PMN Number
- P910023
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA, US
- Reporter Occupation
- OTHER
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. INITIAL REPORTER: COMPANY REPRESENTATIVE.
Description of Event or Problem · 1
IT WAS REPORTED THAT DEVICE WAS POST PACED T WAVE OVERSENSING. PATIENT DID NOT RECEIVE THERAPY. DECREASE VENTRICULAR SENSITIVITY WAS RECOMMENDED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 22610 | ELLIPSE DR, DF-4 CONNECTOR | IMPLANTABLE CARDIOVERTER DIFIBRILLATOR | LWS | ST. JUDE MEDICAL, INC. CRMD | CD2311-36Q |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 55 YR |