ENDEAVOR SPRINT RX CORONARY STENT SYSTEM
Report
- Report Number
- 2953200-2010-00790
- Event Type
- Death
- Date Received
- May 7, 2010
- Date of Event
- June 9, 2010
- Report Date
- November 21, 2013
- Manufacturer
- MEDTRONIC CARDIOVASCULAR GALWAY
- Product Code
- NIQ
- PMA / PMN Number
- P060033
- Removal / Correction Number
- NA
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Occupation
- PHYSICIAN
- Health Professional
- Yes
Narratives
(B)(4).
AN ENDEAVOR SPRINT RX DRUG-ELUTING STENT WAS IMPLANTED TO THE DISTAL LAD. AN ENDEAVOR SPRINT STENT WAS IMPLANTED TO THE PROXIMAL LAD. A SECOND ENDEAVOR SPRINT STENT WAS IMPLANTED OVERLAPPING THE FIRST STENT TO TREAT A DISSECTION IN THE PROXIMAL LAD. (MFR REPORT# 2953200-2010-00790, 2953200-2010-00791, 2953200-2010-00792). THE PATIENT WAS DISCHARGED THE FOLLOWING DAY. AT THE 30 DAY FOLLOW UP THE PATIENT HAD STABLE ANGINA. APPROXIMATELY 4 MONTHS POST INDEX PROCEDURE THE PATIENT HAD INSTENT RESTENOSIS AND SUSPECTED STENT THROMBOSIS. TVR WAS PERFORMED TO THE PROXIMAL LAD. THE INVESTIGATOR STATED THAT THERE WAS A DEFINITE RELATIONSHIP TO THE STUDY DEVICE AND NO RELATIONSHIP TO THE PROCEDURE. APPROXIMATELY 5 1/2 MONTHS POST INDEX PROCEDURE THE PATIENT WAS HOSPITALIZED DUE TO A GASTROINTESTINAL BLEED. THE PATIENT HAD 2 DAY RECTAL BLEEDING, MEDICATION WAS ADMINISTERED AND A COLONOSCOPY WAS PERFORMED. THE PATIENT RECOVERED WITH TREATMENT. THE INVESTIGATOR STATED THAT THERE WAS NO RELATIONSHIP OF THE GASTROINTESTINAL BLEED AND THE STUDY STENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | ENDEAVOR SPRINT RX CORONARY STENT SYSTEM | NIQ | MEDTRONIC CARDIOVASCULAR GALWAY |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 85 YR | Female | Required Intervention| D |