Hoyer HPL500 HPL500-EL-S2Recalls & reported problems
Joerns Healthcare, LLC · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00857268006813), received between Aug 29, 2025 and Aug 29, 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. 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
- Break1
Patient problems
- Bruise/Contusion1
- Fall1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 29, 2025Break; Break
IT WAS REPORTED TO THE MANUFACTURER, BY THE END USER, PER THE END USER, THAT PATIENT CALLED TO REPORT AN INCIDENT THAT INVOLVED A FLOOR LIFT. THE PATIENT REPORTED THAT THE BOTTLE SCALE ALLEGEDLY GAVE WAY AND PATIENT FELL TO THE FLOOR. PATIENT WENT TO THE HOSPITAL BUT ONLY HAD BUMPS AND BRUISES AND WAS RELEASED. COMPLAINT #(B)(4) AND RA #84098042 WAS ENTERED INTO OUR SYSTEM TO HAVE THE LIFT RETURNED FOR INVESTIGATION. AS OF THIS WRITING, THE LIFT HAS NOT BEEN RETURNED.
Patient problems: Bruise/Contusion; Fall
MAUDE report 22920160 ↗
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- Medline MDS400ELBMedline Industries, Inc. · Lift, patient, non-ac-powered79 reports
- MEDLINE MDS88200HLMedline Industries, Inc. · Lift, patient, non-ac-powered77 reports
- Likorall™ overhead lift 3121001Liko AB · Lift, patient, non-ac-powered1 recall24 reports
- Likorall™ overhead lift 3124050Liko AB · Lift, patient, non-ac-powered1 recall18 reports
- Viking™ XL mobile lift 2040043Liko AB · Lift, patient, non-ac-powered1 recall14 reports
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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