Class II
Medical Device Recall: Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US
ARJOHUNTLEIGH POLSKA Sp. z.o.o. · March 10, 2026
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.
Distribution
US Nationwide distribution.
States Affected
NATIONWIDE
Quantity Affected
119 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1811-2026
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.