Apex Lifts HOY-PRESENCEWSC-SRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00810055881499), received between May 4, 2025 and May 4, 2025 — classified as 1 malfunction.

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.

• MalfunctionMay 4, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  IT WAS REPORTED TO THE MANUFACTURER, BY THE END USER, PER THE END USER, THAT DURING A LIFT TRANSFERRING A PATIENT FROM A WHEELCHAIR TO A BED THE STRAP FAILED. SUSIE STATES THE STRAP WAS A HOYER SLING, AND THE STRAPS WERE NOT FRAYED. FORTUNATELY, THERE WERE NO INJURIES WHEN ASKED WHETHER THE LIFT AND SLING HAD BEEN REMOVED FROM SERVICE AND ASKING FOR PICS SHOWING THAT FAILED STRAP, SHE MENTIONED THE SLING WAS DISPOSED OF. WHEN ASKING FOR AN ITEM OR MODEL # OF THE SLING, SHE WAS NOT CERTAIN, BUT SAID THE SLING WAS BLUE. I CONFIRMED IF THE MAIN COLOR OF THE SLING WAS BLUE OF IF ONE OF THE COLORS ON THE SLING WAS BLUE - SHE RESTATED THE MAIN COLOR OF THE SLING WAS BLUE. I THEN TOLD HER THAT SLING WAS LIKELY NOT A HOYER SLING AS THE PREDOMINANT COLOR ON OUR SLINGS IS GREY WITH COLOR ACCENTS FOR IDENTIFICATION. COMPLAINT # (B)(4) WAS ENTERED INTO OUR SYSTEM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21955877 ↗