Medline Industries, Inc. DYNJ41565JRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10195327555672), received between May 8, 2024 and May 8, 2024 — classified as 2 injuries.

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.

• InjuryMay 8, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  ACCORDING TO THE CUSTOMER ON (B)(6), "PROVIDER NOTED AFTER CESAREAN SECTION THAT PATIENT HAD A MACULAR RASH IN THE DISTRIBUTION OF C-SECTION DRAPE."

  Patient problems: Rash

  MAUDE report 19267384 ↗
• InjuryMay 8, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  ACCORDING TO THE CUSTOMER ON 1/12, "MORNING OF POST OP DAY 4 THERE WAS NOTED TO BE ERYTHEMA SURROUNDING THE INCISION AS WELL AS PERINEUM AND SPREADING TO LOWER ABDOMEN."

  Patient problems: Erythema; Itching Sensation; Pain; Rash

  MAUDE report 19267209 ↗