ORCA?
Received May 27, 2026 · Event occurred Mar 31, 2026
Report 3005099803-2026-02134 · MDR key 25301325
Device
Generic name
Endoscope Channel Accessory
Manufacturer
Boston Scientific CorporationModel number
SUV-617-50Catalog number
SUV-617-50
Lot number
0038400303
Product problems
- Physical Resistance/Sticking
Patient
NA · Unknown
- No Clinical Signs, Symptoms or Conditions
Narrative
Description of Event or Problem
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT TEN ORCA VALVES WERE USED DURING AN ESOPHAGOGASTRODUODENOSCOPY (EGD) PROCEDURE FOR THE TREATMENT OF GERD ON (B)(6) 2026. DURING THE PROCEDURE, THE PHYSICIAN OBSERVED THAT THE RED SUCTION BUTTON BECAME STUCK IN THE DEPRESSED POSITION AFTER INSERTION. THE PHYSICIAN ATTEMPTED TO REMOVE AND REINSERT THE BUTTON SEVERAL TIMES, BUT THE ISSUE PERSISTED. A NEW PACK OF BUTTONS OF THE SAME TYPE WAS THEN OPENED AND USED TO COMPLETE THE PROCEDURE. NO PATIENT COMPLICATIONS WERE REPORTED AS A RESULT OF THIS EVENT.
Additional Manufacturer Narrative
BLOCK H6: IMDRF DEVICE CODE A0509 CAPTURES THE REPORTABLE EVENT OF SUCTION BUTTON STICKING. BLOCK H11: AT THIS TIME THE DEVICE IS CURRENTLY UNDERGOING TECHNICAL ANALYSIS. THE INVESTIGATION IS NOT YET COMPLETE. A SUPPLEMENTAL REPORT WILL BE SUBMITTED ONCE THE RESULTS ARE AVAILABLE. 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.
Remedial action
- Recall