Medline Industries, Inc. DYNJ82072Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10195327165468), received between Jul 16, 2024 and Jul 16, 2024 — 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.

• MalfunctionJul 16, 2024Connection Problem; Connection Problem

  ACCORDING TO THE CUSTOMER, "THEY ARE NOT SURE WHICH IS CAUSING THE ISSUE SINCE IT JUST WINDS ITSELF OFF AND THEY THINK IT MIGHT BE THE SYRINGE, BUT NOT SURE, OTHER CUSTOMERS HAVE REPORTED THIS SO I BELIEVE WE HAVE AN ANSWER AT THIS POINT. THEY HAD TO OPEN NEW MANIFOLD AND CONTROL SYRINGES."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19750763 ↗