Medline Industries, Inc. DYNJTRANS84Recalls & reported problems
Medline Industries, Inc. · PRESSURE MONITORING KIT - 84IN · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10889942582631), received between Apr 11, 2024 and Sep 28, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Fluid/Blood Leak” (2 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
- Fluid/Blood Leak2
- Leak/Splash1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 28, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50920756 ↗MalfunctionSep 23, 2026Fluid/Blood Leak
It was reported that "THE LINE HAS BEEN PRIMED, PRESSURE BAG IS SET, WHEN THEY GO TO FLUSH THE LINE INTO THE PATIENT THEY ARE USING IT SPRAY OUT OF THE SIDE OF THE STOPCOCK. ALSO, LEAKING FROM LITTE KNOB YOU TURN TO REDIRECT FLOW."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50869632 ↗MalfunctionApr 11, 2024Leak/Splash; Leak/Splash
ACCORDING TO THE CUSTOMER, "ARTERIAL LINES/ PRESSURE MONITORING MALFUNCTIONS AT THE STOP COCK, LEAKS FLUID, AND BREAKS OFF BEHIND THE HOLDER".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19089830 ↗
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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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