Medline Industries, Inc. DYNDC3023BRecalls & reported problems
Medline Industries, Inc. · PORT DRESSING KIT · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10195327538064), received between Sep 16, 2025 and Sep 16, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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
- Break1
- Material Fragmentation1
- Material Integrity Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 16, 2025Break; Material Fragmentation; Material Integrity Problem; Break; Material Fragmentation; Material Integrity Problem
ACCORDING TO THE FACILITY, THE SALINE SYRINGE FOUND IN THE KIT WAS BROKEN AND SHARP. PER THE FACILITY, "BROKEN PRODUCT WAS FOUND BEFORE IT WAS USED ON PATIENT."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23062424 ↗
Other Central venous catheter tray devices
- Medline Industries, Inc. DYNJ70141MBMedline Industries, Inc. · Central venous catheter tray4 recalls1 report
- Medline Industries, Inc. DYNJ70152MBMedline Industries, Inc. · Central venous catheter tray4 recalls0 reports
- Medline Industries, Inc. DYNJ80643Medline Industries, Inc. · Central venous catheter tray3 recalls0 reports
- 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.
How reports and recalls are matched · Editorial policy · Report an error on this page