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Medical Device

Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US

Recall date: 2026-04-22 · Source: FDA_DEVICE
Brand / Firm
ARJOHUNTLEIGH POLSKA Sp. z.o.o.
Product
Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US
Reason for recall
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.
Units affected
119 units
Description
Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US
View official recall notice →