inforMED
InjuryODF

SPYSCOPE ACCESS AND DELIVERY CATHETER

Received Aug 11, 2009 · Event occurred Jul 9, 2009

Report 3005099803-2009-03810 · MDR key 1436711

Device

Model number

M00546230

Catalog number

4623

Lot number

OML9050503

Product problems

  • Other (for use when an appropriate device code cannot be identified)

Patient

18 YR

  • Therapy/non-surgical treatment, aborted/stopped
  • Therapy/non-surgical treatment, additional

Narrative

Description of Event or Problem

NOTE: THIS REPORT PERTAINS TO ONE OF TWO COMPLAINTS THAT OCCURRED DURING THE SAME PROCEDURE. REFER TO MANUFACTURER REPORT # 3005099803-2009-03811 FOR THE OTHER ASSOCIATED DEVICE INFORMATION. IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A SPYSCOPE ACCESS AND DELIVERY CATHETER AND A SPYGLASS DIRECT VISUALIZATION PROBE WERE USED DURING AN ERCP (ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY) WITH ELECTROHYDRAULIC LITHOTRIPSY (EHL) PROCEDURE PERFORMED IN 2009. ACCORDING TO THE COMPLAINANT, DIFFICULTY WAS ENCOUNTERED WHILE ADVANCING THE SPYPROBE THROUGH THE SPYSCOPE. THE SPYPROBE APPEARED TO BECOME STUCK AT THE SPYSCOPE TIP. THE SPYSCOPE WAS REMOVED FROM THE PATIENT, BUT THE SPYPROBE STILL COULD NOT BE ADVANCED THROUGH THE CHANNEL. THE PROCEDURE WAS NOT COMPLETED DUE TO THIS EVENT. HOWEVER, A BILIARY STENT WAS PLACED TO ALLOW DUCT DRAINAGE UNTIL THE PROCEDURE COULD BE RE-SCHEDULED. 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.

Additional Manufacturer Narrative

THE DEVICE HAS BEEN RECEIVED FOR ANALYSIS. UPON COMPLETION OF THE FAILURE ANALYSIS OF THE COMPLAINT DEVICE, IF THERE IS ANY FURTHER RELEVANT INFORMATION FROM THAT REVIEW, A SUPPLEMENTAL MEDWATCH WILL BE FILED.