Warning
ARJOHUNTLEIGH POLSKA Sp. z.o.o. Recalls Arjo Tenor mobile passive patient lift
This is a Class II recall. This product may cause temporary health problems or pose a slight threat of a serious nature.
Source: FDA
WarningRecall #Z-1811-2026Medical Device
ARJOHUNTLEIGH POLSKA Sp. z.o.o. Recalls Arjo Tenor mobile passive patient lift
ARJOHUNTLEIGH POLSKA Sp. z.o.o. · Class II — Moderate Risk
Product Description
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.
FDA Classification
Class II — Moderate Risk
A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Distribution
US Nationwide distribution.
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
411 Press Analysis
ARJOHUNTLEIGH POLSKA Sp. z.o.o. has recalled a medical device that the FDA classified as Class II affecting 119 units. The recall was initiated on March 10, 2026. An internal component of the actuators in a certain production batch may not meet the required mechanical strength. It was distributed in US Nationwide distribution. Class II recalls involve products that might cause a temporary health problem or pose only a slight threat of a serious nature. Consumers should discontinue use and contact the firm.
Sources: FDA openFDA Enforcement Database
This recall appears in: Other Injury Hazards.