Medline Industries, Inc. DYNJ52304BRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10889942830329), received between Jul 31, 2018 and Jul 31, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Material Fragmentation” (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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryJul 31, 2018Material Fragmentation

  IT WAS REPORTED THAT DURING THE SET-UP OF AN UNIDENTIFIED PROCEDURE, FOREIGN PARTICULATE WAS FOUND ON A LAP SPONGE AND INSIDE OF A PITCHER. REPORTEDLY, THE UNIDENTIFIED PROCEDURE WAS CANCELLED AND THE PATIENT WAS REQUIRED TO RETURN TO HAVE IT COMPLETED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7734581 ↗