Arjohuntleigh Magog Inc.
FDA adverse event reports naming Arjohuntleigh Magog Inc. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ARJOHUNTLEIGH MAGOG INC..
- Total reports
- 1,280
- Deaths
- 57
- Injuries
- 433
- Malfunctions
- 781
Reports per year
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
Recent recalls
- 2023-05-24Open, ClassifiedProcess control
Arjo Portable Scale Adaptor, Model Number 700.05725; accessory intended to be used in combination with compatible patient lifting equipment
Some Arjo Portable Scale Adaptors have been assembled with straps that have a potential to detach.
- TerminatedNonconforming Material/Component
Arjo Flat Dynamic Positioning System (DPS) - Product Usage: used in conjunction with passive clip slings is designed for resident transfer in a homecare setting, at nursing homes and other assisted living centers. Please note that the DPS can be utilized only if affixed to ceiling lift or passive floor lift.
Risk of Sling Clip breakage while in use with obsolete Flat Dynamic Positioning System (DPS)
- TerminatedUnder Investigation by firm
Maxi Sky 1000 (Arjo) and V10 (BHM) Bariatric Ceiling Rail - Mounted Lift with measuring function
The spreader bar can disconnect from the scale bottom attachment.
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