Medline DYNDTNBC21G7Recalls & reported problems
Medline Industries, Inc. · BLD COLL SET, 21GX0.75", 7IN TUBING · 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 10193489010404), received between Jul 8, 2024 and Sep 24, 2026 — classified as 3 malfunctions.
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.
Reports received per month
Most reported problems
Device problems
- Break1
- Fluid/Blood Leak1
- Insufficient Device Problem Information1
- Material Separation1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Hemorrhage/Blood Loss/Bleeding1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 24, 2026Material Separation
It was reported that "The pigtail line separated from the proximal end of the white luer hub, which I've never seen happen. Bleeding from the open end of the line occurred and required attention by the staff member drawing blood to gain control."
Patient problems: Hemorrhage/Blood Loss/Bleeding
MAUDE report 50885369 ↗MalfunctionSep 14, 2026Break; Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50764735 ↗MalfunctionJul 8, 2024Insufficient Device Problem Information; Insufficient Device Problem Information
CUSTOMER FEEDBACK: THE HOSE IS SEPARATED FROM THE WHITE CONNECTOR SEAT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19687258 ↗
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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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