Lift, Patient, Non-ac-powered
Arjohuntleigh Magog, Inc.'s record for this product code
MDR events1,333All time
Recalls3All time
510(k) clearances0All time
Recent MDR events
1,333 adverse event reports on file
- MAXI SKY 2Jul 21, 2026Malfunction9681684-2026-00063
- MAXI MOVE 5Jul 21, 2026Malfunction9681684-2026-00062
- MIRANTI LIFTJul 20, 2026MalfunctionMW5190852
- MAXI MOVEJul 15, 2026Malfunction9681684-2026-00059
- MAXI MOVE 5Jul 14, 2026Malfunction9681684-2026-00061
- MAXI 500Jul 14, 2026Malfunction9681684-2026-00057
- SARA FLEXJul 10, 2026Death9681684-2026-00055
- SARA FLEXJul 10, 2026Death1419652-2026-00104
- SARA FLEXJul 10, 2026Injury9681684-2026-00058
- SARA FLEXJul 10, 2026Injury1419652-2026-00106
Recalls
3 recall events for this product code
- Open, ClassifiedMay 24, 2023
Some Arjo Portable Scale Adaptors have been assembled with straps that have a potential to detach.
View FDA record ↗ - TerminatedUnknown
Risk of Sling Clip breakage while in use with obsolete Flat Dynamic Positioning System (DPS)
View FDA record ↗ - TerminatedUnknown
The spreader bar can disconnect from the scale bottom attachment.
View FDA record ↗
510(k) clearances
0 clearances for this product code
No 510(k) clearances on file for Arjohuntleigh Magog, Inc. under this product code.