Salem Sump 8888266122 (UDI 10884521004696)Recalls & reported problems
Cardinal Health, Inc. · Dual Lumen Stomach Tube,Anti-Reflux Valve · Class 2
All models of Salem Sump (28)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10884521004696), received between Mar 27, 2023 and Mar 27, 2023 — classified as 1 injury.
The most frequently reported specific device problem is “Break” (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
- Break1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 27, 2023Break; Break
THE CUSTOMER REPORTED THAT THE VERY TIP OF TUBING BROKE OFF. PER ADDITIONAL INFORMATION RECEIVED, THE PIECE THAT BROKE OFF WAS LEFT IN THE PATIENT AND THE DOCTOR HAD TO GO BACK IN AND TAKE IT OUT.
Patient problems: Foreign Body In Patient
MAUDE report 16624170 ↗
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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