Medline DYNDTNBC23G7Recalls & reported problems
Medline Industries, Inc. · BLD COLL SET, 23GX0.75", 7IN TUBING · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10193489010428), received between Sep 9, 2026 and Sep 28, 2026 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Difficult or Delayed Activation” (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
- Difficult or Delayed Activation2
- Detachment of Device or Device Component1
- Fluid/Blood Leak1
- Retraction Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
- Discomfort2
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 28, 2026Retraction Problem
It was reported that "THE NEEDLES ARE NOT GOING BACK INTO THE SAFETY SLEEVE."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50913572 ↗MalfunctionSep 24, 2026Detachment of Device or Device Component
It was reported that "When engaging the safety on the device, the needle fell off and onto the floor."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50884312 ↗MalfunctionSep 17, 2026Difficult or Delayed Activation
It was reported that "There is a safety issue with how hard they are to slide the protective sleeve up on the used needle. Some are so hard to slide, that we cannot use the safety slide at all."
Patient problems: Discomfort
MAUDE report 50804750 ↗MalfunctionSep 16, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50786115 ↗MalfunctionSep 9, 2026Difficult or Delayed Activation
It was reported that "There is a safety issue with how hard they are to slide the protective sleeve up on the used needle. Some are so hard to slide, that we cannot use the safety slide at all."
Patient problems: Discomfort
MAUDE report 50691016 ↗
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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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