MEDLINE DYNDTA1540Recalls & reported problems
Medline Industries, Inc. · IV ADMIN SET, SECONDARY, 40" W / HANGER · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 8
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 10888277655881), received between Mar 22, 2023 and Sep 29, 2026 — classified as 8 malfunctions.
The most frequently reported specific device problem is “Disconnection” (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.
Reports received per month
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available3
- Disconnection1
- Failure to Disconnect1
- Fluid/Blood Leak1
- Infusion or Flow Problem1
- Loose or Intermittent Connection1
- Mechanical Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions8
Recent adverse event reports
The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2026Infusion or Flow Problem
It was reported that "I have a faulty secondary tubing that was not pumping medication properly."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50932501 ↗MalfunctionSep 21, 2026Failure to Disconnect
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50839376 ↗MalfunctionSep 21, 2026Fluid/Blood Leak; Mechanical Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50838743 ↗MalfunctionSep 18, 2026Disconnection
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50829970 ↗MalfunctionMay 1, 2026Loose or Intermittent Connection
THE TUBING BECAME DISCONNECTED FROM THE DRIP CHAMBER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25062133 ↗MalfunctionMar 22, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
MEDICATION LEAKING FROM IV SET.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16592613 ↗MalfunctionMar 22, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
MEDICATION LEAKING FROM IV SET.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16592379 ↗MalfunctionMar 22, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
MEDICATION LEAKING FROM IV SET.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16591831 ↗
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- Autosoft XC 1001681Unomedical A/S · Set, Administration, Intravascular1 death4,216 reports
- Minimed™ Quick-set™ MMT-397AUnomedical A/S · Set, Administration, Intravascular19 deaths4,134 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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