Arjohuntleigh Magog

FDA Regulatory Profile

Arjohuntleigh Magog appears in FDA public data with 6 recalls, 0 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent recall (Z-1629-2023, Class II) was initiated on February 17, 2023.

Summary

Total Recalls
6
510(k) Clearances
0
Inspections
1
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-1629-2023Class IIArjo Portable Scale Adaptor, Model Number 700.05725; accessory intended to be used in combination wiFebruary 17, 2023
Z-2479-2021Class IIMaxi Sky 1000 (Arjo) and V10 (BHM) Bariatric Ceiling Rail - Mounted Lift with measuring functionMarch 4, 2021
Z-1100-2021Class IIArjo Flat Dynamic Positioning System (DPS) - Product Usage: used in conjunction with passive clip slOctober 6, 2020
Z-0802-2019Class IIARJOHUNTLEIGH GETINGE GROUP, RotoProne Therapy System, Model Number 209800December 19, 2018
Z-2661-2018Class IIQ-Connect 272 KG Scale used with Maxi Sky 2 ceiling lift The Scale is intended to be used with paFebruary 12, 2018
Z-2660-2018Class IIQuick Connect 272 KG Scale used with Maxi Sky 2 ceiling lift The Scale is intended to be used witFebruary 12, 2018