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ARJOHUNTLEIGH POLSKA Sp. z.o.o. recalls Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US
Recalled April 22, 2026 · FDA recall Z-1811-2026 · ARJOHUNTLEIGH POLSKA Sp. z.o.o
Hazard
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. · FDA Class II
Units
119 units
Sold at
US Nationwide distribution.
Description
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.
Product
Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US
Manufacturer(s)
ARJOHUNTLEIGH POLSKA Sp. z.o.o.
Made in
Poland
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →