Medline Industries, Inc. DYNJ15331MRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10195327425340), received between Jul 10, 2025 and Jul 17, 2025 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Leak/Splash” (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.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 17, 2025Leak/Splash; Leak/Splash

  ACCORDING TO THE FACILITY "THE SYRINGES ARE LEAKING AT THE HUB".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22530138 ↗
• MalfunctionJul 10, 2025Fluid/Blood Leak; Leak/Splash; Fluid/Blood Leak; Leak/Splash

  IT WAS REPORTED THAT DURING CATARACT SURGERY SET UP AND PRIOR TO USE, LEAKS WERE NOTED WHILE FILLING AND PRIMING SYRINGES "WHERE THE CANNULA ATTACHES/SCREWS INTO THE SYRINGE."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22469212 ↗