Arjo Tenor Mobile Patient Lift
Arjo Tenor patient lifts (Models KHA1000 US, KHA1010 US) recalled for actuator failure risk causing sudden arm drop.
Stop using the affected Tenor lift immediately. Contact Arjo for inspection and repair of the actuator components. Do not attempt to lift patients until the device has been serviced and verified safe.
Why it was recalled
An internal component of the actuators in a certain production batch may not meet the required mechanical strength. This could result, in the worst case scenario, in a sudden loss of the actuator's ability to hold the load, leading to rapid and uncontrolled downward movement of the lifting arm.
How to identify it
UPC 05055982787758 05055982787710
Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US
Where it was sold
Distributed in US.
Official source
Editorial summary by Recall Canary · last updated 2026-04-27 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification