Medline DYNDSBCN21GRecalls & reported problems
Medline Industries, Inc. · SAFETY BLOOD COLLECTION NEEDLE 21GX1.25" · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 17
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 17 adverse event reports that list this exact device (DI 10193489007879), received between Sep 9, 2026 and Sep 30, 2026 — classified as 17 malfunctions.
The most frequently reported specific device problem is “Material Twisted/Bent” (5 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
- Material Twisted/Bent5
- Detachment of Device or Device Component3
- Fluid/Blood Leak3
- Connection Problem2
- Failure to Align2
- Protective Measures Problem2
- Activation Problem1
- Break1
Patient problems
- No Clinical Signs, Symptoms or Conditions15
- Exposure to Body Fluids1
- Needle Stick/Puncture1
Recent adverse event reports
The 17 most recent of 17 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Detachment of Device or Device Component
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50951338 ↗MalfunctionSep 22, 2026Fluid/Blood Leak
It was reported that "the customer drawing blood from a patient and blood leaking from the distal needle into the tube holder."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50856114 ↗MalfunctionSep 18, 2026Fluid/Blood Leak; Loose or Intermittent Connection; Retraction Problem
It was reported that "The needle cover is not coming back down over the needles and blood is continuing to flow out of the needle after removing the tube."
Patient problems: Exposure to Body Fluids
MAUDE report 50819124 ↗MalfunctionSep 17, 2026Connection Problem; Detachment of Device or Device Component
It was reported that "When they movethe safety cover to the sde of the device, t pulls the cap off the needle before they are reay ti remove it. The rubber over the needle that fits in the blood tube holder is too rigid and difficult to hold a blood collection tube on. The resistance from the rubber pushes the tube off the needle unexpectedly.".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50805317 ↗MalfunctionSep 17, 2026Break
It was reported that "Safety clip breaks while in use."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50804345 ↗MalfunctionSep 16, 2026Detachment of Device or Device Component
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50794040 ↗MalfunctionSep 15, 2026Connection Problem; Activation Problem
It was reported that the tops come off as you are screwing the needle into the hub. The safety does not engage properly; the tubes will pop off the needle while filling the tubes.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50771311 ↗MalfunctionSep 14, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50764173 ↗MalfunctionSep 12, 2026Failure to Align
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50746766 ↗MalfunctionSep 11, 2026Material Too Soft/Flexible
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50736651 ↗MalfunctionSep 11, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50732987 ↗MalfunctionSep 10, 2026Material Twisted/Bent; Protective Measures Problem
It was reported that the needles are bent and the safety doesn¿t cover the needle.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50717816 ↗MalfunctionSep 10, 2026Material Twisted/Bent
It was reported that "The luer is bending when we try to insert the tube and sometimes when the tube is removed, blood in the needle squirts out."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50715154 ↗MalfunctionSep 10, 2026Material Twisted/Bent
It was reported that the unit is bent at the bevel.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50714673 ↗MalfunctionSep 9, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50698792 ↗MalfunctionSep 9, 2026Protective Measures Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50698586 ↗MalfunctionSep 9, 2026Failure to Align
Patient problems: Needle Stick/Puncture
MAUDE report 50696978 ↗
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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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