Maxi Move KMCEUN-DRecalls & reported problems
Arjohuntleigh AB · Maxi Move w/DPS Manual, & SCALE, Extra Low Height - Mobile Floor Lifter - Safe working load of 500 lb / 227 kg. · Class 1
- Adverse event reports
- 2
- Deaths reported
- 2
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 05055982763042), received between Mar 28, 2025 and Mar 28, 2025 — classified as 2 deaths.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (2 reports).
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.
Reports received per month
Most reported problems
Device problems
- Insufficient Device Problem Information2
- Use of Device Problem1
Patient problems
- Physical Entrapment2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
DeathMar 28, 2025Use of Device Problem; Insufficient Device Problem Information; Use of Device Problem; Insufficient Device Problem Information
THE EVENT OCCURRED IN JANUARY WHEN A PATIENT WAS RECOVERING AFTER ABDOMINAL SURGERY. ACCORDING TO THE CUSTOMER, A NURSE USED THE DPS FUNCTION TO LOWER THE SPREADER BAR BUT ALLEGEDLY STOPPED TOO LATE, CAUSING THE SPREADER BAR TO PRESS AGAINST THE PATIENT'S ABDOMEN. THE PATIENT PASSED AWAY 24 HOURS LATER. CURRENTLY, THERE IS NO INFORMATION INDICATING ANY FAILURES OF THE ARJO DEVICE. THE CUSTOMER INSPECTED THE DEVICE INTERNALLY AFTER THE EVENT.
Patient problems: Physical Entrapment
MAUDE report 21717740 ↗DeathMar 28, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
THE EVENT OCCURRED IN JANUARY WHEN A PATIENT WAS RECOVERING AFTER ABDOMINAL SURGERY. ACCORDING TO THE CUSTOMER, A NURSE USED THE DPS FUNCTION TO LOWER THE SPREADER BAR BUT ALLEGEDLY STOPPED TOO LATE, CAUSING THE SPREADER BAR TO PRESS AGAINST THE PATIENT'S ABDOMEN. THE PATIENT PASSED AWAY 24 HOURS LATER. CURRENTLY, THERE IS NO INFORMATION INDICATING ANY FAILURES OF THE ARJO DEVICE. THE CUSTOMER INSPECTED THE DEVICE INTERNALLY AFTER THE EVENT.
Patient problems: Physical Entrapment
MAUDE report 21717736 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.