Medline Industries, Inc. DYNDV1938Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10889942117291), received between Dec 27, 2021 and Dec 27, 2021 — classified as 2 injuries.

The most frequently reported specific device problem is “Loose or Intermittent Connection” (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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryDec 27, 2021Loose or Intermittent Connection

  IT WAS REPORTED THAT THE HUB CAME UNDONE WHILE CONNECTED TO THE PATIENT PRIOR TO STARTING THE CONTRAST AND THE PATIENT BLED ON THE TABLE AND THE FLOOR (TOTAL AMOUNT OF BLOOD LOSS UNKNOWN).

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

  MAUDE report 13090665 ↗
• InjuryDec 27, 2021Loose or Intermittent Connection

  IT WAS REPORTED THAT THE HUB CAME UNDONE WHILE CONNECTED TO THE PATIENT PRIOR TO STARTING THE CONTRAST AND THE PATIENT BLED ON THE TABLE AND THE FLOOR (TOTAL AMOUNT OF BLOOD LOSS UNKNOWN).

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

  MAUDE report 13090636 ↗