MAUDE Adverse Event Report: AOMORI OLYMPUS CO., LTD. SINGLE USE ELECTROSURGICAL KNIFE KD-655

Model Number	KD-655Q
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Bowel Perforation (2668)
Date of Event	07/30/2023
Type of Reportable Event	Serious Injury
Event or Problem Description
Olympus reviewed the following literature titled "diagnostic and therapeutic strategies for colorectal tumor with positive muscle-retracting sign." literature summary: endoscopic submucosal dissection (esd) for colorectal tumors with positive muscle-retracting (mr) sign often results in incomplete resection or discontinuation owing to the difficulty of submucosal dissection.The present study aimed to evaluate the usefulness of endoscopic ultrasonography (eus) in diagnosing the mr sign and performing esd using the pocket-creation method (pcm).Thirty-six cases of colorectal tumors with positive mr sign during esd between january 2015 and december 2021 were retrospectively reviewed.Cases were divided into two groups: 1) the conventional method (cm) group, comprising 29 cases, and 2) the pcm group with seven cases, in which preoperative eus and esd using pcm were performed.Treatment outcomes were compared between the groups.The diagnostic yield of eus for the mr sign was evaluated among large sessile tumors >20 mm in which preoperative eus was performed.Type of adverse events/number of patients: intraoperative perforation requiring clips to close - 10 patients.Delayed perforation ¿ 1 patient.Discontinued esd leading to emergency surgery ¿ 8 patients.This literature article requires 5 reports.The related patient identifiers are as follows: pcf-q260azi: (b)(6), pcf-h290ti: (b)(6), kd-650q: (b)(6), kd-655q: (b)(6), kd-612q: (b)(6).This medical device report is for patient identifier (b)(6).There is no report of any olympus device malfunction in any procedure described in this study.
Additional Manufacturer Narrative
The investigation is ongoing.A supplemental report will be submitted upon completion of the investigation or if additional information is received.
Additional Manufacturer Narrative
This report is being supplemented to provide additional information based on the legal manufacturer's final investigation.The device history record was unable to be reviewed for this device since the serial and/or lot number was not provided.However, olympus only releases products to market that meet all manufacturing specifications and final product release criteria.Based on the results of the investigation, the relationship between the device and the adverse event cannot be confirmed.There was no complaint reported on the subject device.There is no evidence of an olympus device malfunction.Therefore, the root cause cannot be determined.Olympus will continue to monitor field performance for this device.

• Brand Name: SINGLE USE ELECTROSURGICAL KNIFE KD-655
• Common Device Name: SINGLE USE ELECTROSURGICAL KNIFE
• Manufacturer (Section D): AOMORI OLYMPUS CO., LTD.; 2-248-1 okkonoki; kuroishi-shi, aomori 036-0 357; JA 036-0357
• Manufacturer (Section G): AOMORI OLYMPUS CO., LTD.; 2-248-1 okkonoki; kuroishi-shi, aomori
• Manufacturer Contact: todd brill ; 800 west park drive; westborough, MA 01581 ; 5082077661
• MDR Report Key: 17748792
• Report Number: 9614641-2023-01321
• Device Sequence Number: 4184373
• Product Code: KNS
• UDI-Device Identifier: 04953170405631
• UDI-Public: 04953170405631
• Combination Product (Y/N): N
• Initial Reporter Country: JA
• PMA/510(K) Number: K171158
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Other,Foreign,Study,Literature,Health Professional,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 09/29/2023

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Model Number: KD-655Q
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 08/17/2023
• Supplement Date Received by Manufacturer: 09/27/2023
• Initial Report FDA Received Date: 09/14/2023
• Supplement Report FDA Received Date: 09/29/2023
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: PCF-H290TI; PCF-Q260AZI
• Outcome Attributed to Adverse Event: Required Intervention; Life Threatening
• Patient Sex: Unknown