ARJOHUNTLEIGH POLSKA Sp. z.o.o. Recall
Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US
Updated March 10, 2026
ARJOHUNTLEIGH POLSKA Sp. z.o.o. is recalling Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US. 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.
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
Am I affected
You may be affected if you own this product. Check the brand, model, and lot/date codes listed in the recall against your item.
What to do right now
Voluntary: Firm initiated
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
- Source
- FDA
- Category
- Medical Devices
- Recall ID
- fda-Z-1811-2026
- Classification
- Class II
- Recalled
- March 10, 2026
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