MalfunctionFSA

MAXI 500

Received Jul 14, 2026 · Event occurred Jun 13, 2026

Report 9681684-2026-00057 · MDR key 25811184

Device

Generic name

Lift, Patient, Non-ac-powered

Manufacturer

Arjohuntleigh Magog Inc.

Model number

Product problems

Device Tipped Over

Patient

84 YR · Female

Hematoma
Pain
Swelling/ Edema