Medline Industries, Inc. DYNDA2892BRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10195327348441), received between Aug 15, 2025 and Aug 15, 2025 — classified as 1 injury.

The most frequently reported specific device problem is “Gas/Air Leak” (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.

• InjuryAug 15, 2025Gas/Air Leak; Gas/Air Leak

  ACCORDING TO THE FACILITY, ON (B)(6) 2025, "THE LOCKING MECHANISM ON THE CHEST TUBE FELL OFF AND OPENED AT THE SLIGHTEST TOUCH, CAUSING AN AIR LEAK. THE AIR LEAK WAS REPAIRED WITH VASELINE GAUZE AND TEGADERM, BUT WE WERE UNABLE TO PLACE THE ALTEPLASE AND DORNASE AS ORDERED."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22817545 ↗