TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM
Report
- Report Number
- 2134265-2008-03115
- Event Type
- Injury
- Date Received
- October 23, 2008
- Date of Event
- September 26, 2008
- Report Date
- September 29, 2008
- Manufacturer
- BOSTON SCIENTIFIC
- Product Code
- NIQ
- PMA / PMN Number
- P030025
- Removal / Correction Number
- NA
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FL, US
- Reporter Occupation
- PHYSICIAN
Narratives
THE COMPLAINANT INDICATED THAT THE DEVICE WILL NOT BE RETURNED FOR EVAL; THEREFORE A FAILURE ANALYSIS OF THE COMPLAINT DEVICE COULD NOT BE COMPLETED. A REVIEW OF THE BATCH HISTORY, HISTORICAL TRENDING, AND SIMILAR COMPLAINT TRENDING REVIEW FOR THE PRODUCT FAMILY WILL BE CONDUCTED. IF THERE IS ANY FURTHER RELEVANT INFO FROM THAT REVIEW, A SUPPLEMENTAL MEDWATCH WILL BE FILED.
SAME CASE AS: 2134265-2008-03114. IT WAS REPORTED THAT POST A CORONARY DRUG ELUTING STENTING TREATMENT PROCEDURE, VESSEL DISSECTION AND THROMBOSIS OCCURRED. AN UNK SIZE TAXUS EXPRESS2 DRUG ELUTING STENT WAS DEPLOYED IN THE 80% STENOSED LESION LOCATED IN THE MILDLY CALCIFIED, MILDLY TORTUOUS DISTAL RIGHT CORONARY ARTERY (RCA). AN UNK SIZE TAXUS EXPRESS2 DRUG ELUTING STENT WAS DEPLOYED IN THE 80% STENOSED LESION LOCATED IN THE NON-CALCIFIED, NON-TORTUOUS PROXIMAL RIGHT CORONARY ARTERY (RCA). THE STENTS WERE WELL APPOSED. FOUR HOURS POST THE INITIAL INTERVENTION, THE PT PRESENTED WITH CHEST PAIN. THE DISTAL STENT HAD CAUSED A DISSECTION RESULTING IN A THROMBOSIS. THE PHYSICIAN RESTENTED WITH A PROMUS STENT AND THE PT TOLERATED THIS WELL. PT STATUS REPORTED AS "OK".
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM | NIQ STENT, CORONARY, DRUG-ELUTING | NIQ | BOSTON SCIENTIFIC |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention |