MAUDE Adverse Event Report: OLYMPUS MEDICAL SYSTEMS CORP. EVIS LUCERA DUODENOVIDEOSCOPE

Model Number JF-260V

Device Problem Adverse Event Without Identified Device or Use Problem (2993)

Patient Problems Hemorrhage/Bleeding (1888); Pancreatitis (4481)

Event Date 05/15/2022

Event Type  Injury  

Manufacturer Narrative

This report is being submitted to report the user's experiences and investigation findings.The devices referenced in this report were not returned to olympus for physical evaluation.The device history record (dhr) for the complaint devices could not be reviewed since the serial numbers were not provided.Olympus does not ship any device that does not meet all design and safety specifications.Conclusion: no malfunction of any olympus device was reported in any procedure described in this article.From the information reported, it is.

Event Description

It is reported in the literature titled ¿application and usefulness of a new eight-wire basket catheter for endoscopic extraction of small common bile duct stones: a retrospective multicenter study,¿ patients experienced adverse events after procedures using multiple olympus devices.Case with patient identifier (b)(6) reports jf:260v.Case with patient identifier (b)(6) reports tjf-q290v.Case with patient identifier (b)(6) reports b-v231p-a.Objectives: distally located small common bile duct stones are often difficult to treat or grasp endoscopically.Therefore, multiple devices, such as baskets or balloon catheters, are frequently used in such cases.However, itis desirable to use a single device for stone extraction from the perspective of cost-effectiveness.In this multicenter study, we evaluated the efficacy of a new eight-wire basket catheter for extracting small (=10 mm) common bile duct stones.Methods: we retrospectively analyzed the records of 144 patients who underwent stone extraction using the eight-wire basket catheter for common bile duct stones=10 mm.The success rate of complete stone extraction and the risk factors for the difficulty in stone extraction with the eight-wire catheter alone were mainly evaluated.Results: the success rate of stone extraction with the eight-wire catheter alone was 86.1%.The final rate of complete stone extraction was 98.0%.The mean of the maximum diameter of the common bile duct and the largest stone dimension were 10.5±3.5, and 5.1±2.1 mm, respectively.Common bile duct diameter=12 mm and stone diameter=6 mm were identified as independent risk factors for the difficulty in stone extraction with the eight-wire catheter alone.Conclusions: the success rate of the new eight-wire basket for small common bile duct stone extraction was acceptable.The device is beneficial and could be used from the start for the extraction of small stones<6 mm.Complications occurred in 2.7%, in the form of post-ercp pancreatitis in two patients and post-est bleeding in two patients.The severity of the complications was mild in all cases.There is no report of olympus device malfunction reported in any procedure described in this study.

Manufacturer Narrative

This report is being supplemented to provide additional information received, from the authoring physician and the legal manufacturer's final investigation.The authoring physician confirmed, there was no olympus device malfunction.The contingencies were common ones that can occur with endoscopic retrograde cholangiopancreatography (ercp), and are unlikely to have been caused by the olympus devices.The serial lot numbers of the olympus devices used in the study are unknown.Based on the results of the final investigation, it is likely that the reported event is an accident or a complication associated with a surgical procedure using the subject device.However, the specific root cause could not be determined at this time.Olympus will continue to monitor field performance for this device.

• Brand Name: EVIS LUCERA DUODENOVIDEOSCOPE
• Type of Device: DUODENOVIDEOSCOPE
• Manufacturer (Section D): OLYMPUS MEDICAL SYSTEMS CORP.; 2951 ishikawa-cho; tokyo-to, hachioji-shi 192-8 507; JA 192-8507
• Manufacturer Contact: kazutaka matsumoto ; 2951 ishikawa-cho; hachioji-shi, tokyo-to 192-8-507 ; JA 192-8507 ; 426425177
• MDR Report Key: 15086396
• MDR Text Key: 296413796
• Report Number: 8010047-2022-12095
• Device Sequence Number: 1
• Product Code: FDT
• Combination Product (y/n): N
• Reporter Country Code: JA
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Other,Foreign,Study,Literature,Health Professional
• Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date: 11/23/2022

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 07/22/2022
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Device Model Number: JF-260V
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Date Manufacturer Received: 11/11/2022
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Is the Device Single Use?: No
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Reuse
• Patient Sequence Number: 1
• Patient Outcome(s): Other