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High risk Medical DevicesClass II

Arjo Tenor Patient Lift Recall

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

Updated March 10, 2026

Certain Arjo Tenor mobile patient lifts may have a defective internal component in the actuator that could suddenly lose its ability to hold the load, causing the lifting arm to drop rapidly and uncontrollably. This poses a serious risk of injury to patients and caregivers.

Is the ARJOHUNTLEIGH POLSKA Sp. z.o.o. recalled? Yes. This product was recalled by FDA on March 10, 2026. Details below.

What is recalled

Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US, from Arjohuntleigh Polska Sp. z.o.o. The affected units are from a specific production batch with internal actuator component defects.

Am I affected

You are affected if you own or operate an Arjo Tenor mobile patient lift with Model Number KHA1000 US or KHA1010 US. Check the model number on your device label.

What to do right now

Stop using the affected lift immediately. Contact Arjohuntleigh or your equipment supplier for instructions on how to return, repair, or replace the device. Do not attempt to use this lift until it has been inspected and cleared.

The 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.

Brands affected

ARJOHUNTLEIGH POLSKA Sp. z.o.o.
Source
FDA
Category
Medical Devices
Recall ID
fda-Z-1811-2026
Classification
Class II
Recalled
March 10, 2026
Read the official notice

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