MEDLINE OGBCS23GTRecalls & reported problems
Medline Industries, Inc. · BLD COLL SET, 23GX0.75, HOLDER · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10197344112111), received between Sep 28, 2026 and Sep 28, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Loose or Intermittent Connection” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Loose or Intermittent Connection2
- Restricted Flow rate1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 28, 2026Loose or Intermittent Connection
It was reported that "the replacement butterfly needles are difficult to use. The phlebotomists said that after they connect the holder and begin the draw, they noticed that the vacutainer tubes do not stay very well in the holder and that the blood flow is very slow. Some said that they feel resistance from the vaccum and tube will pop out from the assembly."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50916014 ↗MalfunctionSep 28, 2026Restricted Flow rate; Loose or Intermittent Connection
It was reported that "the replacement butterfly needles are difficult to use. The phlebotomists said that after they connect the holder and begin the draw, they noticed that the vacutainer tubes do not stay very well in the holder and that the blood flow is very slow. Some said that they feel resistance from the vaccum and tube will pop out from the assembly."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50915985 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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