Medline Industries, Inc. DYKF1045Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10889942865062), received between Nov 2, 2020 and Nov 2, 2020 — classified as 1 malfunction.

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

• MalfunctionNov 2, 2020Break

  IT WAS REPORTED A GAIT BELT CLASP BROKE WHILE ASSISTING PATIENT FROM THE BED TO THE CHAIR. PATIENT FELL AND HIT HIS HEAD. PATIENT WAS ADMITTED TO THE LOCAL HOSPITAL OBSERVATION AND CAT SCAN WAS COMPLETED.

  Patient problems: Fall

  MAUDE report 10771459 ↗