ARJOHUNTLEIGH POLSKA Sp. z.o.o. has recalled 119 Arjo Tenor mobile passive patient lifts because an internal component can fail due to insufficient mechanical strength. This defect can cause the lifting arm to suddenly and uncontrollably drop while holding a patient, posing a severe risk of falls and impact injuries. The recall affects Model Numbers KHA1000 US and KHA1010 US manufactured in Poland and distributed nationwide.
The lift's actuator may lose its ability to hold a load, resulting in the patient being dropped rapidly. This could lead to serious physical trauma or death for patients being transported or lifted.
Units from a specific production batch where the internal component of the actuator may not meet strength requirements.
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES · Raw API Response
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