APEX HOY-ADVANCE-HRecalls & reported problems
Joerns Healthcare, LLC · HOYER ADVANCE LIFTER · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00810055880058), received between May 27, 2025 and May 27, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Unintended System Motion” (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.
Reports received per month
Most reported problems
Device problems
- Unintended System Motion1
Patient problems
- Fall1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 27, 2025Unintended System Motion; Unintended System Motion
IT WAS REPORTED TO THE MANUFACTURER, BY THE END USER, PER THE END USER, THAT (B)(6) (VENDOR) STATES CLIENT CALLED DUE TO MAST BEING DAMAGED, THERE HAD BEEN AN INCIDENT WHERE THE LIFT 'FELL OVER' WHILE ATTEMPTING TO LIFT HIM BUT THERE WERE NO INJURIES. (B)(6) STATES THAT (HE RESIDENT/CLIENT STATED THAT PRIOR TO STARTING LIFT, THEY HAD LIFTED THE MAST UP AND OUT OF BASE, AND THAT MAST BENT WHEN IT TIPPED FORWARD DURING LIFT. COMPLAINT # (B)(4). WAS ENTERED INTO OUR SYSTEM.
Patient problems: Fall
MAUDE report 22090787 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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