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.
Recall at a glance
- Quantity recalled
- 119 units
Why it was recalled
Arjo is recalling Tenor mobile passive patient lifts, Model Numbers KHA1000 US and KHA1010 US, due to a defect in internal actuator components that may fail to hold the load, potentially causing rapid and uncontrolled downward movement of the lifting arm.
Is mine affected?
Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.
Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US
- UDI-DI
- 05055982787758, 05055982787710
Where it was sold
Distributed nationwide.
Timeline
- Firm initiated recall
- Publicly announced
- Listed on Recall Canary
- Summary updated
Official source
Editorial summary by Recall Canary · summary updated 2026-04-27 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification