Medline Industries, Inc. DYNJAA10634Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10888277786707), received between Nov 14, 2023 and Sep 29, 2026 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Material Separation” (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 29, 2026Material Separation

  It was reported that "In the last three weeks we had 3 incidents with our circuits from Medline. In each of the incidents the circuit broke of right at the connection circuit and filter when pulled at."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50931361 ↗
• MalfunctionSep 22, 2026Material Separation

  It was reported that, "There have been two more reported incidents of the circuit breaking at the filter connection."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50854091 ↗
• MalfunctionNov 14, 2023Material Integrity Problem; Material Integrity Problem

  "NECK OF THE CIRCUIT HAVE SNAPPED OFF AT CONNECTION POINT WITH BACTERIA FILTER".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18133018 ↗