Medline Industries, Inc. DYNJS3018Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10884389099582), received between May 28, 2024 and May 28, 2024 — classified as 1 injury.

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.

• InjuryMay 28, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  ACCORDING TO THE CUSTOMER ON (B)(6) 2024, "IT WAS AN EXPLORATORY LAPAROTOMY WITH REVISION LOOP ILEOSTOMY CASE; THE BELLY WAS OPEN WITH BOWEL EXPOSED. WHILE WAITING FOR AN ASSISTING SURGEON TO ARRIVE THE BLUE TOWELS FROM THE PACK WERE MOISTENED WITH STERILE NORMAL SALINE AND PLACED OVER THE OPEN BELLY. AFTER SURGEON REMOVED BLUE TOWEL AND SAW BLUE LINT-SURGEON IMMEDIATELY AND VIGOROUSLY IRRIGATED THE OPEN ABDOMEN, THEN MANUALLY REMOVED THE REMAINING LINT."

  Patient problems: Insufficient Information

  MAUDE report 19404687 ↗