Nasogastric Sump Tube with PreVent® Anti-Reflux Filter And Lopez Valve® 0056160Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00801741052392), received between Feb 10, 2020 and Dec 5, 2023 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Incorrect Measurement” (1 report).

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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionDec 5, 2023Material Split, Cut or Torn; Material Split, Cut or Torn

  IT WAS REPORTED THAT A CRACK FOUND WHEN INSERTING NASOGASTRIC TUBE INTO PATIENT. THEY OPENED A SECOND TUBE AND THE SAME ISSUE. PULLED ONE WITH A DIFFERENT LOT NUMBER AND NO PROBLEM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18265881 ↗
• MalfunctionFeb 10, 2020Incorrect Measurement; Adverse Event Without Identified Device or Use Problem; Incorrect Measurement

  IT WAS REPORTED THAT THE DIAMETER OF THE CONNECTION ON THE NG TUBE IS SMALL WHICH MAKES DECOMPRESSION OF THE STOMACH MORE DIFFICULT. THE CUSTOMER NOTED THAT THE PATIENT WAS IN THE HOSPITAL FOR SMALL BOWEL OBSTRUCTION AND HAD A NG TUBE IN FOR DECOMPRESSION. THE PATIENT WAS VERY NAUSEATED FOR SEVERAL HOURS, UNRELIEVED BY MEDICATION AND THE NG TUBE WAS BRINGING BACK UP SOME GASTRIC CONTENT BUT NOT A LOT. THE PROVIDER REPORTEDLY HAND IRRIGATED THE NG TUBE VERY FORCEFULLY WITH AT LEAST 2 SYRINGES OF WATER AND AFTER THE SECOND SYRINGE, THE NG TUBE DUMPED OUT 750ML OF GASTRIC CONTENTS.

  Patient problems: Nausea; No Consequences Or Impact To Patient

  MAUDE report 9688408 ↗