Maxi Move KMCLXN-DRecalls & reported problems
Arjohuntleigh AB · Maxi Move w/DPS, Low Height - Mobile Floor Lifter - Safe working load of 500 lb / 227 kg. · Class 1
- 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 05055982764971), received between Jun 11, 2025 and Jun 11, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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.
Reports received per month
Most reported problems
Device problems
- Detachment of Device or Device Component1
- Insufficient Device Problem Information1
Patient problems
- Bruise/Contusion1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 11, 2025Detachment of Device or Device Component; Insufficient Device Problem Information; Detachment of Device or Device Component; Insufficient Device Problem Information
IT WAS REPORTED THAT A PATIENT FELL WHILE BEING TRANSFERRED USING A MAXI MOVE 3 LIFT. THE PATIENT WAS MOVING UNPREDICTABLY IN THE SLING, AND ONE SIDE OF THE SLING BECAME DISCONNECTED FROM THE SPREADER BAR, RESULTING IN A FALL AND HEAD INJURY. THE PATIENT WAS TRANSPORTED TO THE HOSPITAL FOR TREATMENT. NO PRODUCT DEFECTS WERE FOUND. ALL LIFT FUNCTIONS WERE TESTED AND CONFIRMED TO BE WORKING PROPERLY. THE SLING SHOWED NO SIGNS OF DAMAGE.
Patient problems: Bruise/Contusion
MAUDE report 22183535 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.