MAUDE Adverse Event Report: OLYMPUS MEDICAL SYSTEMS CORP. SINGLE USE 3-LUMEN EXTRACTION BALLOON V

Model Number	B-V243Q-A
Medical Device Problem Code	Material Rupture (1546)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Date of Event	06/23/2020
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The device was not returned to olympus for evaluation.The user¿s complaint was not confirmed.The user facility used one balloon that popped when trying to use it on a patient.A different balloon of the same model and lot was used and activated without it rupturing.The procedure was completed with no further issues.No findings available.The cause could not be determined.No further information was reported.A supplemental will be submitted if new information becomes available or the device is returned.
Event or Problem Description
The user facility reported that a balloon popped when trying to inflate it during a patient procedure.There was no patient injury or harm.No additional information was provided.This is file 3 of 3.
Additional Manufacturer Narrative
This supplemental report was submitted to provide additional information to mdr# 8010047-2020-04619.The original equipment manufacturer (oem), performed a device history record review and no abnormalities were noted.No device was returned to the oem, however, an investigation was completed by the oem and determined that there is no manufacturing, material or processing related cause for this failure mode.Based on previous complaints, it was speculated that when the balloon was inflated and quarrying, the rubber of the balloon was damaged at the corner of the stone and the balloon ruptured.However, it was not possible to determine when and what load was applied and the balloon was punctured.Olympus will continue to monitor the field performance of this device.After checking the contents of the instruction manual, the following caution was issued regarding the description related to this event.- confirm that the balloon is completely deflated when inserting the instrument into the endoscope.If the balloon is not deflated completely, the distal end of the instrument may extend from the distal end of the endoscope abruptly.This could cause patient injury, such as perforation, bleeding, or mucous membrane damage, and could damage the endoscope and/or instrument.- do not force to insert the instrument if resistance to insertion is encountered.Reduce the angulation (or lower the forceps elevator if applicable) until the instrument passes smoothly.The use of excessive force causes patient injury, such as perforation, bleeding, or mucous membrane damage.It may also damage the endoscope and/or instrument.- do not advance or extend the instrument abruptly.This could cause patient injury, such as perforation, bleeding, or mucous membrane damage.It could also damage the endoscope and/or instrument.- insert the instrument into the endoscope slowly.Otherwise, the instrument and/or the endoscope may be damaged.

• Brand Name: SINGLE USE 3-LUMEN EXTRACTION BALLOON V
• Common Device Name: SINGLE USE 3-LUMEN EXTRACTION BALLOON
• Manufacturer (Section D): OLYMPUS MEDICAL SYSTEMS CORP.; 2951 ishikawa-cho; hachioji-shi, tokyo-to 192-8 507; JA 192-8507
• MDR Report Key: 10297659
• Report Number: 8010047-2020-04619
• Device Sequence Number: 19035530
• Product Code: LQR
• UDI-Device Identifier: 04953170368721
• UDI-Public: 04953170368721
• Combination Product (Y/N): N
• Initial Reporter State: PA
• Initial Reporter Country: US
• PMA/510(K) Number: K091495
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,user f
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 11/06/2020

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Model Number: B-V243Q-A
• Device Lot Number: 9ZV
• Was Device Available for Evaluation?: No
• Was the Report Sent to FDA?: No
• Initial Date Received by Manufacturer: 06/23/2020
• Supplement Date Received by Manufacturer: 10/09/2020
• Initial Report FDA Received Date: 07/20/2020
• Supplement Report FDA Received Date: 11/06/2020
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1