Medline Industries, Inc. DYNJRA1994Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10195327188856), received between May 13, 2025 and Sep 30, 2026 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Break” (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 30, 2026Break

  Patient problems: Twitching

  MAUDE report 50948703 ↗
• MalfunctionSep 17, 2026Break

  It was reported that "the syringes in his support trays are breaking when he is in use. The plunger is snapping into pieces. He said this is happening frequently."

  Patient problems: Discomfort

  MAUDE report 50804646 ↗
• MalfunctionMay 13, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  THE SEALS ARE BREAKING ON THE PLUNGERS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22009667 ↗