FDA Adverse Event Injury Summary report: N

TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM

MDR report key: 1904278 · Received November 22, 2010

Report

Report Number
2134265-2010-05091
Event Type
Injury
Date Received
November 22, 2010
Report Date
October 25, 2010
Manufacturer
BOSTON SCIENTIFIC - MAPLE GROVE
Product Code
NIQ
PMA / PMN Number
P030025
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IA, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

LITERATURE CITATION: SHAMMAS, NICOLAS W, MD AND GAIL A. SHAMMAS, RN; MICHAEL JERIN, PHD; ANUP PARIKH, KATERINE COIN; ERIC DIPPEL, MD; PETER SHARIS, MD; JON ROBKEN, MD. TREATMENT OF LEFT MAIN CORONARY TRIFURCATION LESIONS WITH THE PACLITAXEL DRUG-ELUTING STENT: MID-TERM OUTCOMES FROM A TERTIARY MEDICAL CENTER. J INVASIC CARDIOL 2009; 21: 321-325. IF IMPLANTED, GIVE DATE: BETWEEN (B)(6) 2006 AND (B)(6) 2007. DEVICE EVALUATED BY MANUFACTURER- IT IS INDICATED THAT THE DEVICE WILL NOT BE RETURNED FOR EVALUATION; THEREFORE A FAILURE ANALYSIS OF THE COMPLAINT DEVICE COULD NOT BE COMPLETED. THE BATCH NUMBER IS UNKNOWN AND THE MANUFACTURING RECORDS FOR THE COMPLAINT DEVICE COULD NOT BE REVIEWED. IF THERE IS ANY FURTHER RELEVANT INFORMATION IS RECEIVED, A SUPPLEMENTAL MEDWATCH WILL BE FILED. (B)(4).

Description of Event or Problem · 1

IT WAS REPORTED VIA A JOURNAL ARTICLE THAT POST A STENTING TREATMENT PROCEDURE, STENT THROMBOSIS OCCURRED. THE TARGET LESION WAS LOCATED AT A LEFT MAIN TRIFURCATION. AN UNKNOWN TAXUS STENT WAS IMPLANTED AND WAS POST DILATED WITH KISSING BALLOONS. AFTER AN UNSPECIFIED TIME THE PATIENT HAD DEFINITE STENT THROMBOSIS POST PROCEDURE AND WAS RETREATED SUCCESSFULLY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM CORONARY DRUG-ELUTING STENT NIQ BOSTON SCIENTIFIC - MAPLE GROVE UNK432

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention