ARJOHUNTLEIGH POLSKA Sp. z.o.o. recalls Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US

Recall date

March 10, 2026

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-1811-2026

FDA classification

Class II

Brand / firm

ARJOHUNTLEIGH POLSKA Sp. z.o.o.

Sold / distributed

US Nationwide distribution.

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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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