Medline Industries, Inc. DYNDV1719CRecalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10889942916405), received between Mar 21, 2023 and Sep 22, 2026 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Loss of or Failure to Bond” (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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 22, 2026Loss of or Failure to Bond

  It was reported that "Backing window is coming off, Tegaderm sticky piece coming off with it. Not sticking correctly."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50856401 ↗
• MalfunctionSep 11, 2026Loss of or Failure to Bond

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50735913 ↗
• MalfunctionMar 21, 2023Inadequacy of Device Shape and/or Size; Inadequacy of Device Shape and/or Size

  IV CLOTTED OFF REQUIRING AN ADDITIONAL IV TO BE STARTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16583762 ↗