MEDLINE ENFIT9000NSRecalls & reported problems
Medline Industries, Inc. · QUICK SWITCH VALVE,NON-STERILE · Class 2
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 10193489012552), received between Sep 22, 2026 and Sep 30, 2026 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Break” (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.
Reports received per month
Most reported problems
Device problems
- Break4
- Crack1
- Fluid/Blood Leak1
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.
MalfunctionSep 30, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50950037 ↗MalfunctionSep 30, 2026Break
It was reported that "When going to flush the tube, before uncapping one of the ports a crack noticed where the luer lock is. Another port used which ended up breaking."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50946685 ↗MalfunctionSep 25, 2026Break; Fluid/Blood Leak
It was reported that "The tip of the switch valve connector is breaking off at the screw end of the feeding tube." "However, the connection can be leaky, especially when pushing medications through the switch valve."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50897487 ↗MalfunctionSep 22, 2026Break; Crack
It was reported that "PORT WHERE NEEDLE IS INSERTED IS CRACKED, ABOUT A WEEK AGO."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50852426 ↗
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- Salem Sump 7771610ECardinal Health, Inc. · Gastrointestinal Tubes with Enteral Specific Connectors1 death18 reports
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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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