Medline Industries, Inc. DYNJ30320FRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10193489424171), received between Aug 12, 2026 and Aug 14, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Electrical /Electronic Property Problem” (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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 14, 2026Electrical /Electronic Property Problem

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50260943 ↗
• MalfunctionAug 12, 2026Material Separation

  It was reported that inner seal broken (THL's separated).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50221020 ↗