EndoVive Jejunal Feeding Tube M00566350Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 08714729786252), received between Sep 13, 2018 and Mar 23, 2023 — classified as 1 injury, 3 malfunctions.

The most frequently reported specific device problem is “Obstruction of Flow” (2 reports).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 23, 2023Obstruction of Flow; Obstruction of Flow

  IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT AN ENDOVIVE JEJUNAL FEEDING TUBE WAS USED DURING A GASTROSTOMY JEJUNOSTOMY PROCEDURE PERFORMED ON (B)(6) 2023. THE JEJUNAL TUBE BECAME OBSTRUCTED ON (B)(6) 2023. A NEW ENDOVIVE JEJUNAL FEEDING TUBE WAS PLACED. THERE WERE NO REPORTED PATIENT COMPLICATIONS AS A RESULT OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16597344 ↗
• MalfunctionMar 22, 2023Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT AN ENDOVIVE JEJUNAL FEEDING TUBE WAS USED DURING A GASTROSTOMY JEJUNOSTOMY PROCEDURE PERFORMED ON (B)(6) 2023. IT WAS REPORTED ON (B)(6) 2023 THE G-TUBE WAS NO LONGER ATTACHED TO THE ADAPTER OF THE ENDOVIVE JEJUNAL FEEDING TUBE. A NEW ENDOVIVE JEJUNAL FEEDING TUBE WAS PLACED. THERE WERE NO REPORTED PATIENT COMPLICATIONS AS A RESULT OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16592917 ↗
• InjuryMay 17, 2022Migration; Migration

  IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT AN ENDOVIVE STANDARD PEG KIT PUSH METHOD AND ENDOVIVE JEJUNAL FEEDING TUBE WERE USED DURING A PERCUTANEOUS ENDOSCOPIC GASTROSTOMY PLACEMENT PROCEDURE ON (B)(6) 2022. POST PROCEDURE, THE ENDOVIVE JEJUNAL FEEDING TUBE DETACHED FROM THE ENDOVIVE PEG TUBE AND MIGRATED INTO THE STOMACH. UPON X-RAY, IT WAS CONFIRMED THE TUBE WAS IN THE GASTRIC CAVITY. THE PHYSICIAN REMOVED THE TUBE AND A NEW ENDOVIVE STANDARD PEG KIT PUSH METHOD AND ENDOVIVE JEJUNAL FEEDING TUBE WERE PLACED. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14418300 ↗
• MalfunctionSep 13, 2018Obstruction of Flow; Obstruction of Flow

  IT WAS REPORTED TO BOSTON SCIENTIFIC THAT AN ENDOVIVE JEJUNAL FEEDING TUBE WAS USED DURING A PROCEDURE. THE PROCEDURE DATE IS UNKNOWN. ACCORDING TO THE COMPLAINANT, THE JEJUNAL TUBE CLOGGED. ATTEMPTS TO OBTAIN ADDITIONAL INFORMATION REGARDING THE CIRCUMSTANCES SURROUNDING THIS EVENT HAVE BEEN UNSUCCESSFUL TO DATE. SHOULD ADDITIONAL RELEVANT DETAILS BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7872855 ↗