ENDEAVOR RESOLUTE RX CORONARY SYSTEM
Report
- Report Number
- 2953200-2010-00676
- Event Type
- Death
- Date Received
- April 21, 2010
- Date of Event
- January 7, 2010
- Report Date
- March 22, 2010
- Manufacturer
- MEDTRONIC CARDIOVASCULAR GALWAY
- Product Code
- NIQ
- PMA / PMN Number
- P060033
- Removal / Correction Number
- NA
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IS
- Reporter Occupation
- PHYSICIAN
Narratives
(B) (4): EVAL RESULTS: ROOT CAUSE UNDETERMINED.
THREE ENDEAVOR RESOLUTE RX DRUG-ELUTING STENTS (2.25 MM X 14MM, 2.50MM X 14MM AND 3.50MM X 15MM) (REF MFR REPORT# 2953200-2010-00674, 2953200-2010-006765 WERE INSERTED INTO A PT FOR TREATMENT OF A LEFT MAIN AND LAD. LESION MORPHOLOGY WAS REPORTED AS SMALL CALCIFIED DIFFUSELY DISEASED CORONARY ARTERIES WITH SIGNIFICANT STENOSIS OF THE LEFT MAIN, PROXIMAL CX AND LAD/ORIGIN DIAGONAL. THE LAD/DIAGONAL WERE DILATED WITH GOBA (BALLOON ONLY). FOLLOWING PRE-DILATATION THE 2.25 MM DIAMETER X 14MM LENGTH STENT WAS IMPLANTED AT THE PROXIMAL CX. STENTS WERE IMPLANTED IN THE LEFT MAIN AND ORIGIN LAD, FOLLOWED BY POST DILATATION TO 4MM. THERE WAS A GOOD ANGIOGRAPHIC RESULT. THE POST OPERATIVE COURSE REPORTED EPISODES OF CHEST PAIN, TROPONIN RISE, HEART FAILURE AND COLLAPSE AFTER SEVEN DAYS. IT IS REPORTED THAT THE PT HAD AN EMERGENCY RE-CATHETERIZATION. THE MAIN ARTERIES WERE OPEN BUT NO FILLING OF THE SMALL SIDE BRANCHES WERE OBSERVED. IT IS REPORTED THAT THE PT DIED A WEEK LATER. AN AUTOPSY WAS PERFORMED WHICH SHOWED EXTENSIVE MYOCARDIAL DAMAGE. FOREIGN MATERIAL WAS NOTED TO BE IN THE COLLATERAL ARTERIES. DEVICES NOT REC'D FOR EVAL.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | ENDEAVOR RESOLUTE RX CORONARY SYSTEM | NIQ | MEDTRONIC CARDIOVASCULAR GALWAY | NA | 0001121529 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 58 YR | Death |