Maxi Move KMCLXNRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05055982764438), received between May 7, 2021 and May 7, 2021 — 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.

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 7, 2021Detachment of Device or Device Component; Detachment of Device or Device Component

  ARJO WAS NOTIFIED ABOUT AN EVENT INVOLVING ARJO MAXI MOVE PASSIVE FLOOR LIFT AND PASSIVE CLIP SLING (MODEL NO MAA4000M-L, SERIAL NUMBER (B)(4)). IT WAS REPORTED THAT DURING PATIENT TRANSFER FROM A BEDSIDE TOILET TO A BED, THE CLIP DETACHED FROM A SPREADER BAR ATTACHMENT POINT (LUG). FOLLOWING INFORMATION PROVIDED BY THE CUSTOMER THE SLING CLIP DETACHED WHEN PATIENT, (WHO HAS CEREBRAL PALSY) WAS MOVING A LOT AND HER ARM HIT THE CLIP. AS A CONSEQUENCE OF THE EVENT PATIENT FELL OUT FROM THE SLING AND HIT HER HEAD ON THE CHASSIS LEG OF THE LIFT. THE PATIENT SUSTAINED A SMALL BUMP ON THE HEAD, INJURY WAS ASSESSED AS NOT SERIOUS.

  Patient problems: Head Injury

  MAUDE report 11789161 ↗