FDA Adverse Event Malfunction Summary report: N

SPYSCOPE DS ACCESS & DELIVERY CATHETER

MDR report key: 7323570 · Received March 8, 2018

Report

Report Number
3005099803-2018-00617
Event Type
Malfunction
Date Received
March 8, 2018
Date of Event
February 12, 2018
Report Date
February 12, 2018
Manufacturer
BOSTON SCIENTIFIC - SPENCER
Product Code
FBN
UDI-DI
08714729863236
PMA / PMN Number
K142922
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

THE COMPLAINANT INDICATED THAT THE DEVICE HAS BEEN DISPOSED AND WILL NOT BE RETURNED FOR EVALUATION; THEREFORE, A FAILURE ANALYSIS OF THE COMPLAINT DEVICE COULD NOT BE COMPLETED. IF ANY FURTHER RELEVANT INFORMATION IS IDENTIFIED, A SUPPLEMENTAL MDR WILL BE FILED.

Description of Event or Problem · 1

NOTE: THIS REPORT PERTAINS TO ONE OF THREE DEVICES USED DURING THE SAME PROCEDURE. REFER TO MANUFACTURER REPORT# 05099803-2018-00612 FOR THE FIRST SPYSCOPE DIGITAL ACCESS AND DELIVERY CATHETER, 3005099803-2018-00617 FOR THE SECOND SPYSCOPE DIGITAL ACCESS AND DELIVERY CATHETER, AND 3005099803-2018-00589 FOR THE RX CYTOLOGY BRUSH. IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A SPYSCOPE DIGITAL ACCESS & DELIVERY CATHETER AND AN RX CYTOLOGY BRUSH WERE USED IN THE COMMON BILE DUCT (CBD) DURING AN ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY (ERCP) PROCEDURE PERFORMED ON (B)(6) 2018. ACCORDING TO THE COMPLAINANT, DURING THE PROCEDURE, IT WAS NOTICED THAT THE WORKING CHANNEL SLEEVE OF THE SPYSCOPE DS PROTRUDED. A SECOND SPYSCOPE DS WAS USED AND THE WORKING CHANNEL SLEEVE PROTRUDED. REPORTEDLY, NO PART OF THE SPYSCOPE DS DEVICES DETACHED. AN RX CYTOLOGY BRUSH WAS ALSO USED DURING THE PROCEDURE AND THE BRUSH WAS DIFFICULT TO EXTEND AND IT WAS ALSO NOTED THAT THE WIRE INSIDE THE CATHETER BROKE. THE PROCEDURE WAS COMPLETED WITH THE SECOND SPYSCOPE DIGITAL ACCESS AND DELIVERY CATHETER AND THE SAME RX CYTOLOGY BRUSH. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT. THE PATIENT'S CONDITION AT THE CONCLUSION OF THE PROCEDURE WAS REPORTED TO BE FINE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
168866 SPYSCOPE DS ACCESS & DELIVERY CATHETER CHOLEDOCHOSCOPE AND ACCESSORIES, FLEXIBLE/RIGID FBN BOSTON SCIENTIFIC - SPENCER M00546600 21626802 08714729863236

Patients

Seq Age Sex Outcome Treatment
1