Medline DYNDMSN215Recalls & reported problems
Medline Industries, Inc. · MULTI-SAMPLE NEEDLE 21GX1" · Class 2
- 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 10193489013313), received between Aug 22, 2024 and Sep 15, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Connection Problem” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Connection Problem2
- Fluid/Blood Leak1
- Unintended Ejection1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Insufficient Information1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 15, 2026Unintended Ejection; Connection Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50777277 ↗MalfunctionSep 14, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50765043 ↗MalfunctionAug 22, 2024Connection Problem; Connection Problem
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.