MAUDE Adverse Event Report: BOSTON SCIENTIFIC CORPORATION Orca?; Endoscope Channel Accessory

Model Number	SUV-617
Medical Device Problem Code	Physical Resistance/Sticking (4012)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	03/10/2026
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Block h6: imdrf device code a0509 captures the reportable event of suction button sticking.Block h11: investigation result: with the information available, boston scientific could not confirm the reported event of suction button sticking.Device technical analysis: the device was not returned for analysis; therefore, a technical analysis could not be performed.Investigation conclusion: based on the available information, the most probable cause of the reported event cannot be established due to lack of evidence.Additionally, without proper evaluation of the device, it remains unknown the most probable cause that contributed to the event.Since the investigation findings do not lead to a clear conclusion about the cause of the reported events, "cause not established" is selected as the most probable cause for the complaint.On (b)(6) 2026, boston scientific initiated a field safety corrective action (fsca - boston scientific reference: (b)(4)) that included the removal of orca single use air/water and suction valves associated with batch number 38400303 due to increased reports of suction button sticking issues.A communication was sent out to materials managers/health care professionals on (b)(6) 2026, with instructions to immediately stop further use or distribution of orca single use air/water and suction valves associated with batch number 38400303, remove the devices from inventory, and segregate them in a secure location until they can be returned to boston scientific.Boston scientific will continue to closely monitor and trend similar events and associated risks, as outlined in our quality systems process.
Event or Problem Description
It was reported to boston scientific corporation that an orca valve was used during a colonoscopy procedure performed on (b)(6) 2026.During the procedure, the suction button became stuck in the depressed position.The physician removed the button, dip it in water, and reinsert it; however, the valve continued to stick.The procedure was completed using another suction button.No patient complications were reported as a result of this event.The patient was reported to have fully recovered.

• Brand Name: Orca?
• Common Device Name: Endoscope Channel Accessory
• Manufacturer (Section D): BOSTON SCIENTIFIC CORPORATION; 300 boston scientific way; marlborough MA 01752
• Manufacturer (Section G): Boston Scientific Corporation; model farm road; cork T12 Y K88; EI T12 YK88
• Manufacturer Contact: christina lam ; 300 boston scientific way; marlborough, MA 01752 ; +1(914)571-6918
• MDR Report Key: 25301319
• Report Number: 3005099803-2026-02131
• Device Sequence Number: 13084896
• Product Code: ODC
• UDI-Device Identifier: 00840253111012
• UDI-Public: (01)00840253111012(17)290120(10)38400303
• Combination Product (Y/N): N
• Initial Reporter State: CA
• Initial Reporter Country: US
• PMA/510(K) Number: K160403
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Health Professional,Company Representative
• Initial Reporter Occupation: Other Health Care Professional
• Remedial Action: Recall
• Type of Report: Initial,Followup
• Report Date (Section B): 08/11/2026

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: SUV-617
• Device Catalogue Number: SUV-617
• Device Lot Number: 0038400303
• 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: 04/28/2026
• Supplement Date Received by Manufacturer: 07/14/2026
• Initial Report FDA Received Date: 05/27/2026
• Supplement Report FDA Received Date: 08/12/2026
• Date Device Manufactured: 01/21/2026
• 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
• If action reported to FDA under 21 USC 360i(g), list FDA-assigned Recall Number or include a statement: 3005099803-05112026-002-
• Patient Sequence Number: 1
• Patient Sex: Unknown