MAUDE Adverse Event Report: OLYMPUS MEDICAL SYSTEMS CORPORATION SINGLE USE 3-LUMEN SPHINCTEROTOME

Model Number KD-V411M-0320

Device Problem Break (1069)

Patient Problem No Consequences Or Impact To Patient (2199)

Event Date 03/27/2015

Event Type  malfunction  

Event Description

Olympus medical systems corp (omsc) was informed that during endoscopic sphincterotomy, the cutting wire broke.The doctor completed the procedure with another device.During the investigation, omsc found the plastic coating on the cutting wire was partially missing.There was no report of patient injury regarding this report.

Manufacturer Narrative

The investigation confirmed that the cutting wire was broken and the broken section was melted and burned.Approximately coating was missing for 4mm from the broken point.There were no other abnormalities related to the breakage in the subject device.Also as the checking of the manufacturing record of the same lot, nothing abnormal detected.As the results of the investigation, omsc assumes that the damage of the coating occurred due to contacting w with the forceps elevator of the endoscope.The exposed cutting wire from the damaged coating contacted or came close to the metal part of the forceps elevator while activating the output, which caused spark and a part of the cutting wire became extremely hot, resulting in breakage.The coating broke off and came off from the cutting wire because of the user handling after the cutting wire we broken.This report is being submitted as a medical device report in an abundance of caution.

• Brand Name: SINGLE USE 3-LUMEN SPHINCTEROTOME
• Type of Device: SPHINCTEROTOME
• Manufacturer (Section D): OLYMPUS MEDICAL SYSTEMS CORPORATION; 2951 ishikawa-cho; hachioji-shi 192- 8507; JA 192-8507
• Manufacturer Contact: sasuma nishina ; 2951 ishikawa-cho; hachioji-shi ; JA ; 26425177
• MDR Report Key: 4798236
• MDR Text Key: 16078955
• Report Number: 8010047-2015-00354
• Device Sequence Number: 1
• Product Code: FDR
• Combination Product (y/n): N
• Reporter Country Code: JA
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Health Professional,User Facility
• Reporter Occupation: Not Applicable
• Type of Report: Initial
• Report Date: 04/28/2015

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 05/19/2015
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Other
• Device Model Number: KD-V411M-0320
• Device Lot Number: K4Z18
• Was Device Available for Evaluation?: Yes
• Date Returned to Manufacturer: 04/27/2015
• Date Manufacturer Received: 04/28/2015
• Was Device Evaluated by Manufacturer?: Yes
• Date Device Manufactured: 12/01/2014
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1