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Salem Sump 8888268086 (UDI 10884521007765)Recalls & reported problems

Cardinal Health, Inc. · Dual Lumen Stomach Tube · 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
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10884521007765), received between May 16, 2022 and May 16, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Fluid/Blood Leak” (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

  • Fluid/Blood Leak1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionMay 16, 2022Fluid/Blood Leak; Fluid/Blood Leak

    THE CUSTOMER REPORTED THE FEED WAS LEAKING FROM THE NG TUBE INTO BED. THE LEAKING WAS NOTED WHERE THE NG TUBE BRANCHES OFF AT THE REFLUX LUMEN ON THE TUBE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 14406981 ↗

Other TUBES, GASTROINTESTINAL (AND ACCESSORIES) devices

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Sources and updates

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