ULTRAFLEX PRECISION COLONIC STENT SYSTEM
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
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.
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 |