Salem Sump 7771810Recalls & reported problems
Cardinal Health, Inc. · Dual Lumen Stomach Tube,Multi-functional Port · Class 2
All models of Salem Sump (28)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10884521004566), received between Aug 5, 2021 and Aug 5, 2021 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Crack” (4 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.
Most reported problems
Device problems
- Crack4
- Fluid/Blood Leak3
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 5, 2021Crack; Crack
THE CUSTOMER REPORTED THE 18FR STOMACH TUBE WAS FOUND CRACKED DURING A CHECK. THERE WAS NO PATIENT INVOLVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12281673 ↗MalfunctionAug 5, 2021Crack; Fluid/Blood Leak; Crack; Fluid/Blood Leak
THE CUSTOMER REPORTED THE 18 FR STOMACH TUBES ARE CRACKED/SPLIT AT THE END CREATING LEAKING TUBES ON THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12281548 ↗MalfunctionAug 5, 2021Crack; Fluid/Blood Leak; Crack; Fluid/Blood Leak
THE CUSTOMER REPORTED THE 18 FR STOMACH TUBES ARE CRACKED/SPLIT AT THE END CREATING LEAKING TUBES ON THE PATIENTS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12280979 ↗MalfunctionAug 5, 2021Crack; Fluid/Blood Leak; Crack; Fluid/Blood Leak
THE CUSTOMER REPORTED THE 18FR STOMACH TUBE IS CRACKED/SPLIT AT THE END, CREATING A LEAKING TUBE ON THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12280822 ↗
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.
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