Medline Industries, Inc. DYNJRA1991ARecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10195327306045), received between Sep 11, 2025 and Sep 11, 2025 — classified as 1 malfunction.

The most frequently reported specific device problem is “Connection Problem” (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.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 11, 2025Leak/Splash; Connection Problem; Leak/Splash; Connection Problem

  IT WAS REPORTED THAT "10CC SYRINGES PROVIDED IN THE BLOCK TRAYS LEAK WITH THE PROVIDED 27-GAUGE HYPODERMIC NEEDLE IN THE TRAY." THE CUSTOMER REPORTED THAT "TIGHTENING THE NEEDLE-SYRINGE CONNECTION" PARTIALLY RESOLVES THE LEAKAGE ISSUE BUT CREATES DIFFICULTY REMOVING THE NEEDLE SO THAT IT CAN BE REPLACED WITH A SPINAL NEEDLE TO ACCESS "DEEPER TISSUE."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23033729 ↗