Medline Industries, Inc. DYNJ51615PRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10198459135767), received between Aug 11, 2026 and Aug 11, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Deformation Due to Compressive Stress” (1 report).

1 FDA recall record name this device's identifier, 1 still open.

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.

Recalls naming this device

1. Mar 24, 2026Class IOpen, Classified

   Medline has identified the presence of particulate within the fluid path of the Manifolds.

   Z-2145-2026 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 11, 2026Deformation Due to Compressive Stress; Material Twisted/Bent

  It was reported that (b)(6) is experiencing packs with damaged contrast squeeze lines and kinked/damaged waste bag lines. There has also been damage to the guidewire bowl.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50210292 ↗