Bard® Nasogastric Sump Tube with PreVent® Anti-Reflux Filter 0046163Recalls & reported problems
C. R. Bard, Inc. · Bard® Nasogastric Sump Tube with PreVent® Anti-Reflux Filter · Class 2
All models of Bard Nasogastric Sump Tube with PreVent Anti-Reflux Filter (6)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00801741052330), received between Nov 20, 2025 and Dec 3, 2025 — classified as 2 injuries, 1 malfunction.
The most frequently reported specific device problem is “Migration” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Migration2
- Device Markings/Labelling Problem1
- Unclear Information1
- Use of Device Problem1
Patient problems
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
- Internal Organ Perforation1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 3, 2025Unclear Information; Unclear Information
IT WAS REPORTED THAT THE OG OROGASTRIC TUBE WAS STOCKED AS A PRODUCT REPLACEMENT FOR A PRODUCT THAT HAS EXTERNAL MEASUREMENT MARKINGS, THIS TUBE PRODUCT DID NOT. THE OG TUBE WAS PLACED ON REDACTED DATE AND PRESUMABLY MIGRATED POTENTIALLY CONTRIBUTING TO OR CAUSING GASTRIC PERFORATION REQUIRING EMERGENCY ABDOMINAL SURGERY. CHEMOTHERAPY BEING USED ON THE PATIENT AT THE TIME OF THE EVENT THAT MAY HAVE CAUSED OR CONTRIBUTED TO THE EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23708780 ↗InjuryDec 2, 2025Migration; Migration
IT WAS REPORTED THAT THE OG OROGASTRIC TUBE WAS STOCKED AS A PRODUCT REPLACEMENT FOR A PRODUCT THAT HAS EXTERNAL MEASUREMENT MARKINGS, THIS TUBE PRODUCT DID NOT. THE OG TUBE WAS PLACED ON REDACTED DATE AND PRESUMABLY MIGRATED POTENTIALLY CONTRIBUTING TO OR CAUSING GASTRIC PERFORATION REQUIRING EMERGENCY ABDOMINAL SURGERY. CHEMOTHERAPY BEING USED ON THE PATIENT AT THE TIME OF THE EVENT THAT MAY HAVE CAUSED OR CONTRIBUTED TO THE EVENT.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 23701210 ↗InjuryNov 20, 2025Use of Device Problem; Device Markings/Labelling Problem; Migration
THIS OG [OROGASTRIC] TUBE WAS STOCKED AS A PRODUCT REPLACEMENT FOR A PRODUCT THAT HAS EXTERNAL MEASUREMENT MARKINGS, THIS PRODUCT DOES NOT. THE OG TUBE WAS PLACED ON [REDACTED DATE] AND PRESUMABLY MIGRATED POTENTIALLY CONTRIBUTING TO OR CAUSING GASTRIC PERFORATION REQUIRING EMERGENCY ABDOMINAL SURGERY.
Patient problems: Internal Organ Perforation
MAUDE report 23605143 ↗
Other TUBE, DOUBLE LUMEN FOR INTESTINAL DECOMPRESSION AND/OR INTUBATION devices
- Salem Sump 8888266114Cardinal Health 200, LLC · TUBE, DOUBLE LUMEN FOR INTESTINAL DECOMPRESSION AND/OR INTUBATION2 recalls0 reports
- CARDINAL HEALTH 8888266122ECardinal Health 200, LLC · TUBE, DOUBLE LUMEN FOR INTESTINAL DECOMPRESSION AND/OR INTUBATION1 recall9 reports
- CARDINAL HEALTH 8888266130ECardinal Health 200, LLC · TUBE, DOUBLE LUMEN FOR INTESTINAL DECOMPRESSION AND/OR INTUBATION1 recall7 reports
- Bard® Nasogastric Sump Tube with PreVent® Anti-Reflux Filter with ENFit™ EN0046160C. R. Bard, Inc. · TUBE, DOUBLE LUMEN FOR INTESTINAL DECOMPRESSION AND/OR INTUBATION1 recall7 reports
- Salem Sump 8888266148Cardinal Health 200, LLC · TUBE, DOUBLE LUMEN FOR INTESTINAL DECOMPRESSION AND/OR INTUBATION1 recall5 reports
- Bard® Nasogastric Sump Tube with PreVent® Anti-Reflux Filter with ENFit™ EN0046180C. R. Bard, Inc. · TUBE, DOUBLE LUMEN FOR INTESTINAL DECOMPRESSION AND/OR INTUBATION1 recall5 reports
- Bard® Nasogastric Sump Tube with PreVent® Anti-Reflux Filter 0046160C. R. Bard, Inc. · TUBE, DOUBLE LUMEN FOR INTESTINAL DECOMPRESSION AND/OR INTUBATION54 reports
- Bard® Nasogastric Sump Tube and PreVent® Filter and Lopez Valve® with ENFit™ EN0056140C. R. Bard, Inc. · TUBE, DOUBLE LUMEN FOR INTESTINAL DECOMPRESSION AND/OR INTUBATION1 recall4 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page