FDA Adverse Event Injury Summary report: N

ULTRAFLEX PRECISION COLONIC STENT SYSTEM

MDR report key: 1328249 · Received February 27, 2009

Report

Report Number
3005099803-2009-00856
Event Type
Injury
Date Received
February 27, 2009
Report Date
January 30, 2009
Manufacturer
BOSTON SCIENTIFIC IRELAND, LTD.
Product Code
MQR
PMA / PMN Number
K030769
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IT
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

OTHER (MIGRATION OCCURRED DUE TO SHRINKAGE OF TUMOR). THE SUSPECT DEVICE LOT NUMBER IS UNKNOWN; THEREFORE, THE DEVICE EXPIRATION AND MANUFACTURE DATES ARE UNKNOWN. THE DEVICE IS NOT AVAILABLE, A DEVICE ANALYSIS CANNOT BE PERFORMED; THEREFORE, THE CAUSE OF THE REPORTED EVENT IS UNDETERMINED.

Description of Event or Problem · 1

NOTE: PROCEDURE AND EVENT DATES ARE UNKNOWN. ON JANUARY 30, 2009, A BOSTON SCIENTIFIC CORPORATION EMPLOYEE BECAME AWARE OF A CLINICAL STUDY ARTICLE, "ULTRAFLEX PRECISION COLONIC STENT PLACEMENT FOR PALLIATION OF MALIGNANT COLONIC OBSTRUCTION: A PROSPECTIVE MULTICENTER STUDY" PUBLISHED IN ENDOSCOPY 2007; VOLUME 66 NO. 5: 920-927. THE FOLLOWING INFORMATION WAS DERIVED FROM THIS ARTICLE: AN ULTRAFLEX PRECISION COLONIC SELF-EXPANDING METAL STENT DESIGNED FOR COLORECTAL USE, WAS USED FOR A STENTING PROCEDURE OF PATIENTS WITH MALIGNANT COLONIC OBSTRUCTION. ACCORDING TO THE ARTICLE, THE SEMS MIGRATED TO THE LOWER RECTUM AFTER TWO MONTHS. SEMS WAS REMOVED WITH A SNARE. MIGRATION WAS ATTRIBUTED TO TUMOR REDUCTION AFTER CHEMOTHERAPY. REPLACEMENT SEMS WAS DEEMED UNNECESSARY. THERE IS NO FURTHER INFORMATION FROM THE ARTICLE REGARDING THE STATUS OF THE PATIENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ULTRAFLEX PRECISION COLONIC STENT SYSTEM MQR BOSTON SCIENTIFIC IRELAND, LTD. UNK UNK

Patients

Seq Age Sex Outcome Treatment
1 UNK Other| R