Medline Industries, Inc. DYNJV0264IRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10193489487619), received between May 13, 2021 and May 13, 2021 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Material Fragmentation” (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.

• MalfunctionMay 13, 2021Material Fragmentation

  IT WAS REPORTED, "TWO SEPARATE INCIDENTS IN WHICH, DR. (B)(6) HAD 2 CASES (ONE THIS WEEKEND/ONE THIS AM) WHERE HE HAD TO PICK-OUT FRAGMENTS OF GAUZE FROM THE ABDOMEN".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11822594 ↗
• MalfunctionMay 13, 2021Material Fragmentation

  IT WAS REPORTED, "TWO SEPARATE INCIDENTS IN WHICH, DR. (B)(6) HAD 2 CASES (ONE THIS WEEKEND/ONE THIS AM) WHERE HE HAD TO PICK-OUT FRAGMENTS OF GAUZE FROM THE ABDOMEN."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11822539 ↗