RX CYTOLOGY BRUSH
Received Apr 23, 2019 · Event occurred Apr 2, 2019
Report 3005099803-2019-02116 · MDR key 8540437
Device
Generic name
Endoscopic Cytology Brush
Manufacturer
Boston Scientific CorporationModel number
M00545000Catalog number
4500
Lot number
0023196845
Product problems
- Break
- Defective Device
- Material Deformation
- Material Twisted/Bent
- Break
- Defective Device
- Material Deformation
- Material Twisted/Bent
Patient
Not reported
- No Consequences Or Impact To Patient
- No Consequences Or Impact To Patient
Narrative
Additional Manufacturer Narrative
(B)(6). (B)(4). THE DEVICE HAS NOT BEEN RECEIVED FOR ANALYSIS; THEREFORE, A FAILURE ANALYSIS OF THE COMPLAINT DEVICE COULD NOT BE COMPLETED. IF ANY FURTHER RELEVANT INFORMATION IS IDENTIFIED, A SUPPLEMENTAL MEDWATCH WILL BE FILED.
Description of Event or Problem
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT AN RX CYTOLOGY BRUSH WIREGUIDED WAS PREPPED FOR USE FOR AN ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY (ERCP) PROCEDURE TO BE PERFORMED IN THE BILE DUCT ON (B)(6) 2019. ACCORDING TO THE COMPLAINANT, DURING PREPARATION PRIOR TO THE PROCEDURE, IT WAS NOTED THAT THE BRUSH WAS NOT UNIFORM AND THE BRISTLES WERE NOT IN ORDER. THE PROCEDURE WAS COMPLETED WITH ANOTHER RX CYTOLOGY BRUSH. THERE WAS NO SERIOUS INJURY NOR WERE THERE ANY ADVERSE PATIENT EFFECTS REPORTED AS A RESULT OF THIS EVENT. BOSTON SCIENTIFIC HAS BEEN UNABLE TO OBTAIN ADDITIONAL INFORMATION REGARDING THE CIRCUMSTANCES SURROUNDING THIS EVENT TO DATE. SHOULD ADDITIONAL RELEVANT DETAILS BECOME AVAILABLE A SUPPLEMENTAL REPORT WILL BE SUBMITTED.
Additional Manufacturer Narrative
INITIAL REPORTER FACILITY AND ADDRESS: (B)(6) HOSPITAL. DEVICE PROBLEM CODE 2981 CAPTURES THE REPORTABLE EVENT OF BRUSH BENT. VISUAL ANALYSIS OF THE RETURNED DEVICE REVEALED THAT THE WORKING LENGTH (EXTRUSION AND PULL WIRE) WAS KINKED APPROXIMATELY AT 19CM FROM THE BLACK HEAT SHRINK. THE HANDLE WAS KINKED AND BROKEN (THUMB RING SEPARATED FROM HANDLE CANNULA), BROKEN END HAD EVIDENCE OF BENDING. FUNCTIONAL ANALYSIS REVEALED THAT THE BRUSH WAS UNABLE TO EXTEND WHEN THE HANDLE CANNULA WAS MOVED SIMULATING THE HANDLE ACTUATION. THE DEVICE WAS DISASSEMBLED AND IT WAS OBSERVED THAT THE PULL WIRE WAS KINKED ADJACENT TO THE HANDLE CANNULA JOINT. NO OTHER ISSUES WERE NOTED. IT IS MOST LIKELY THAT HANDLING OR MANIPULATION OF THE DEVICE DURING UNPACKING/PREPPING/TESTING COULD HAVE AFFECTED THE DEVICE INTEGRITY. LIKELY THE FAILURES FOUND (WORKING LENGTH KINKED, HANDLE KINKED/BROKEN) WERE CAUSED DUE TO MANIPULATION AS THE CUSTOMER BRUSHED BACK AND FORTH DURING TESTING/PREPPING. HANDLING AND MANIPULATION OF THE DEVICE CAN LEAD TO KINKING OF THE CATHETER AND PULL WIRE, THIS CONDITION CAN CAUSE DIFFICULTIES TO EXTEND THE BRUSH, FORCE APPLIED TO THE HANDLE IN ORDER TO EXTEND THE BRUSH CAN RESULT IN BENDING THE HANDLE AND KINKING THE PULL WIRE AT HANDLE CANNULA JOINT, CONTINUED ATTEMPTS TO MOVE THE HANDLE CAN RESULT IN HANDLE BREAKAGE. BASED ON THE INFORMATION AVAILABLE AND THE ANALYSIS PERFORMED, THE INVESTIGATION CONCLUSION CODE FOR THE ENCOUNTERED DAMAGES WILL BE DOCUMENTED AS "ADVERSE EVENT RELATED TO PROCEDURE." IN ADDITION, THE PULL WIRE WAS COMPLETELY REMOVED FROM THE DEVICE IN ORDER TO INSPECT THE BRISTLE SECTION, NO VISUAL ISSUES WERE OBSERVED WITH THE BRISTLE SECTION; CONSEQUENTLY, NOT CONFIRMING THE REPORTED ISSUE, THEREFORE THE INVESTIGATION CONCLUSION CODE FOR THE REPORTED EVENT "WHEN THE DEVICE WAS PREPARED, BRUSH WAS NOT UNIFORM, AND ITS HAIR WAS NOT IN ORDER." WILL BE DOCUMENTED AS "NO PROBLEM DETECTED" SINCE THE DEVICE COMPLAINT OR PROBLEM CANNOT BE CONFIRMED. A REVIEW OF THE DEVICE HISTORY RECORD (DHR) WAS PERFORMED AND CONFIRMED THAT THIS DEVICE MET ALL MATERIAL, ASSEMBLY AND PERFORMANCE SPECIFICATIONS AT THE TIME OF RELEASE FOR DISTRIBUTION.
Description of Event or Problem
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT AN RX CYTOLOGY BRUSH WIREGUIDED WAS PREPPED FOR USE FOR AN ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY (ERCP) PROCEDURE TO BE PERFORMED IN THE BILE DUCT ON (B)(6) 2019. ACCORDING TO THE COMPLAINANT, DURING PREPARATION PRIOR TO THE PROCEDURE, IT WAS NOTED THAT THE BRUSH WAS NOT UNIFORM AND THE BRISTLES WERE NOT IN ORDER. THE PROCEDURE WAS COMPLETED WITH ANOTHER RX CYTOLOGY BRUSH. THERE WAS NO SERIOUS INJURY NOR WERE THERE ANY ADVERSE PATIENT EFFECTS REPORTED AS A RESULT OF THIS EVENT. BOSTON SCIENTIFIC HAS BEEN UNABLE TO OBTAIN ADDITIONAL INFORMATION REGARDING THE CIRCUMSTANCES SURROUNDING THIS EVENT TO DATE. SHOULD ADDITIONAL RELEVANT DETAILS BECOME AVAILABLE A SUPPLEMENTAL REPORT WILL BE SUBMITTED.