Medline Industries, Inc. DYNDH1870Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10195327399481), received between Dec 29, 2025 and Dec 29, 2025 — classified as 1 malfunction.

The most frequently reported specific device problem is “Difficult to Flush” (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.

• MalfunctionDec 29, 2025Difficult to Flush; Difficult to Flush

  IT WAS REPORTED THAT "WHEN DOING INJECTIONS, THE RADIOLOGIST ARE STATING THAT THE SYRINGES ARE HARD TO ADMINISTER MEDICATION THROUGH. THEY SAY THE RUBBER STOPPER PIECE ON THE INSIDE IS TOO BIG FOR THE SYRINGE ITSELF RESULTING IN IT BEING HARD TO PUSH/PULL."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23906938 ↗