Medline DYNDSBCN22GRecalls & reported problems
Medline Industries, Inc. · SAFETY BLOOD COLLECTION NEEDLE 22GX1.25" · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 10193489007886), received between Sep 9, 2026 and Sep 17, 2026 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Material Twisted/Bent” (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
- Adverse Event Without Identified Device or Use Problem2
- Material Twisted/Bent2
- Break1
- Detachment of Device or Device Component1
- Fitting Problem1
- Improper or Incorrect Procedure or Method1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
- Needle Stick/Puncture2
- Pain1
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 17, 2026Adverse Event Without Identified Device or Use Problem
Patient problems: Needle Stick/Puncture
MAUDE report 50808514 ↗MalfunctionSep 17, 2026Adverse Event Without Identified Device or Use Problem
It was reported that "This is the 2nd time this account has encountered needle sticks with these safety needles" and "They decided to give them a try again last month and immediately had another finger stick."
Patient problems: Needle Stick/Puncture
MAUDE report 50803422 ↗MalfunctionSep 16, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50789681 ↗MalfunctionSep 14, 2026Detachment of Device or Device Component
It was reported that "the safety device on the needle is popping off during use."
Patient problems: Pain
MAUDE report 50755158 ↗MalfunctionSep 10, 2026Improper or Incorrect Procedure or Method
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50723104 ↗MalfunctionSep 9, 2026Break; Fitting Problem; Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50701657 ↗
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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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