Bard® Nasogastric Sump Tube 0042100Recalls & reported problems
C. R. Bard, Inc. · Bard® Nasogastric Sump Tube · Class 2
All models of Bard Nasogastric Sump Tube (5)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00801741052231), received between Apr 15, 2022 and May 7, 2022 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Material Twisted/Bent” (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
Device problems
- Material Twisted/Bent1
- Tear, Rip or Hole in Device Packaging1
Patient problems
- Hematemesis1
- Hemorrhage/Blood Loss/Bleeding1
- Vomiting1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMay 7, 2022Material Twisted/Bent; Material Twisted/Bent
IT WAS REPORTED THAT DURING GASTRIC DECOMPRESSION (REMOVAL OF GASTRIC SECRETIONS AND GASES), GASTRIC LAVAGE, AND ADMINISTRATION OF NUTRITIONAL SUPPLEMENTS AND MEDICATION, THE STAFF OF THE PEDIATRICS PATIENT CALLED THE DOCTOR BECAUSE OF PATIENT'S CONTINUED BLEEDING AND VOMITING. THE PATIENT HAD AN BARD NASOGASTRIC SUMP TUBE. AN X-RAY WAS COMPLETED, THE DOCTOR NOTED THAT THE BARD NASOGASTRIC SUMP TUBE WAS COILED IN THE ESOPHAGUS. WHEN THE STAFF REMOVED THE BARD NASOGASTRIC SUMP TUBE, IT LOOKED LIKE THERE WAS A DEFECT AT THE BOTTOM AT ONE OF THE HOLES. MEDICAL INTERVENTION IS UNKNOWN.
Patient problems: Hematemesis
MAUDE report 14316941 ↗MalfunctionApr 15, 2022Tear, Rip or Hole in Device Packaging
PEDS PATIENT WHO THE STAFF CALLED THE DOCTOR ABOUT BECAUSE OF CONTINUED BLEEDING AND VOMITING. THE PEDS PATIENT HAD AN BARD NASOGASTRIC SUMP TUBE. AN X-RAY WAS COMPLETED, THE DOCTOR NOTED THAT THE BARD NASOGASTRIC SUMP TUBE WAS COILED IN THE ESOPHAGUS. WHEN THE PEDS STAFF REMOVED THE BARD NASOGASTRIC SUMP TUBE, IT LOOKED LIKE THERE WAS A DEFECT AT THE BOTTOM AT ONE OF THE HOLES.
Patient problems: Hemorrhage/Blood Loss/Bleeding; Vomiting
MAUDE report 14117759 ↗
Other TUBE, NASOGASTRIC devices
- Bard® Nasogastric Sump Tube with Enfit™ EN0042140C. R. Bard, Inc. · TUBE, NASOGASTRIC1 recall4 reports
- Bard® Nasogastric Sump Tube with Enfit™ EN0042120C. R. Bard, Inc. · TUBE, NASOGASTRIC1 recall2 reports
- Bard® Nasogastric Sump Tube with Enfit™ EN0042160C. R. Bard, Inc. · TUBE, NASOGASTRIC1 recall2 reports
- Bard® Nasogastric Sump Tube with Enfit™ EN0042180C. R. Bard, Inc. · TUBE, NASOGASTRIC1 recall2 reports
- Bard® Nasogastric Sump Tube with Enfit™ EN0042100C. R. Bard, Inc. · TUBE, NASOGASTRIC1 recall0 reports
- Bard® Nasogastric Sump Tube 0042160C. R. Bard, Inc. · TUBE, NASOGASTRIC13 reports
- ENFit PU Feeding Tube PFTM5.0P-NCAvanos Medical, Inc. · TUBE, NASOGASTRIC10 reports
- ENFit PU Feeding Tube PFTL6.5P-NCAvanos Medical, Inc. · TUBE, NASOGASTRIC8 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.
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