MalfunctionFSA
MAXI MOVE 5
Received Jul 14, 2026 · Event occurred Apr 20, 2026
Report 9681684-2026-00061 · MDR key 25809747
Device
Generic name
Lift, Patient, Non-ac-powered
Manufacturer
Arjohuntleigh Magog Inc.Model number
KMESSU-M-0-02Product problems
- Unintended Movement
Patient
NA · Female
- Erythema