Medline Industries, Inc. DYNDV2384DRecalls & reported problems
Medline Industries, Inc. · ASED 40 · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10195327335861), received between Apr 12, 2024 and Dec 11, 2025 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Crack” (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
- Crack2
- Device Contamination with Chemical or Other Material2
- Material Integrity Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions5
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 11, 2025Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material
IT WAS REPORTED THAT ON (B)(6) 2025 THERE WAS "STYROFOAM IN SYRINGE". THE CUSTOMER DID NOT REPORT ANY SERIOUS INJURY, MEDICAL INTERVENTION REQUIRED, OR FOLLOW-UP CARE NEEDED AS A RESULT OF THE REPORTED ISSUE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23780218 ↗MalfunctionSep 11, 2025Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material
IT WAS REPORTED THAT THE SYRINGE FROM THE PACK HAD "DEBRIS" ON IT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23027946 ↗MalfunctionJul 16, 2024Crack; Crack
PER THE FACILITY THE SYRINGE WAS CRACKED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19750630 ↗MalfunctionJun 25, 2024Crack; Crack
IT WAS REPORTED THE SYRINGE WAS NOTED TO BE "CRACKED" WHEN OPENING THE KIT REQUIRING THE CUSTOMER "TO OPEN ADDITIONAL SUPPLIES IN ORDER TO COMPLETE THE ORDER".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19606167 ↗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 19098511 ↗
Other Central venous catheter tray devices
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- Medline Industries, Inc. DYNJ63199AMedline Industries, Inc. · Central venous catheter tray3 recalls0 reports
- Medline Industries, Inc. DYNJ66271BMedline Industries, Inc. · Central venous catheter tray3 recalls0 reports
- Medline Industries, Inc. DYNJ55546DMedline Industries, Inc. · Central venous catheter tray3 recalls0 reports
- Medline Industries, Inc. DYNJ68037CMedline Industries, Inc. · Central venous catheter tray2 recalls1 report
- Medline Industries, Inc. DYNJ84239Medline Industries, Inc. · Central venous catheter tray2 recalls0 reports
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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