APEX HML400Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00810055880003), received between Sep 4, 2025 and Sep 4, 2025 — 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. How this data works · Data updated Oct 13, 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.

• MalfunctionSep 4, 2025Break; Break

  IT WAS REPORTED TO THE MANUFACTURER, BY THE END USER, PER THE END USER, THAT CUSTOMER CALLED IN ABOUT A LIFT THAT BROKE WHILE MOVING A RESIDENT. THERE WERE NO INJURIES TO THE RESIDENT OR THE STAFF. THE RESIDENT WAS ONLY 150 LBS AND SAID THAT IT BROKE AT THE FOOT PART WHERE THE LEG SPREAD OPEN WHEN LIFTING THE RESIDENT INTO THE LIFT. CUSTOMER SAID THAT EVERYTHING LOOKED NORMAL WHEN PUTTING IT TOGETHER IN THE LAST FEW DAYS. THERE WERE NO INJURIES TO THE RESIDENT OR THE STAFF. COMPLAINT#: (B)(4) AND RA #84098094 WAS ENTERED INTO OUR SYSTEM TO HAVE THE LIFT RETURNED FOR INVESTIGATION. AS OF THIS WRITING, THE LIFT HAS NOT BEEN RETURNED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22974727 ↗