Medline Industries, Inc. DYNDV1934JRecalls & reported problems
Medline Industries, Inc. · ASED 30 · 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 10195327335854), received between Apr 12, 2024 and Sep 24, 2026 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Contamination” (1 report).
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
- Contamination1
- Crack1
- Insufficient Device Problem Information1
- Material Integrity Problem1
- Melted1
- Missing Information1
Patient problems
- No Clinical Signs, Symptoms or Conditions6
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 24, 2026Melted
MalfunctionAug 27, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
MalfunctionJul 1, 2025Missing Information; Missing Information
ACCORDING TO THE FACILITY "WE OPENED THE KIT AND WERE NOT ABLE TO USE THE SYRINGE AS THE NUMBERS ARE ILLEGIBLE".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22370427 ↗MalfunctionJul 25, 2024Contamination; Contamination
IT WAS REPORTED A BLACK PARTICLE WAS FOUND INSIDE THE SYRINGE WHEN THE CUSTOMER WAS "OPENING THE KIT".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19833875 ↗MalfunctionJul 16, 2024Crack; Crack
PER THE FACILITY THE SYRINGE WAS CRACKED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19750365 ↗MalfunctionApr 12, 2024Material Integrity Problem; Material Integrity Problem
ACCORDING TO THE FACILITY "THE TECHNICIAN SET UP THEIR STERILE FILED AND WHEN THEY WENT TO USE THE SYRINGE, THEY WERE UNABLE TO, DUE TO ITS CONDITION".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19098318 ↗
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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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