MEDLINE DYNDV1614CRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10653160361213), received between May 5, 2026 and Sep 29, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Complete Blockage” (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 16, 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.

• MalfunctionSep 29, 2026Fluid/Blood Leak

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50938885 ↗
• MalfunctionMay 5, 2026Complete Blockage

  VALVE ABOVE SYRINGE STUCK CLOSED. LUER LOCK TIGHT AS CAN BE. NO FLUID WILL FLOW, VALVE DOES NOT OPEN.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25089088 ↗