Arjo Tenor mobile patient lift recalled for actuator component failure risk
Stop using Arjo Tenor patient lift models KHA1000, KHA1010
Certain Arjo Tenor mobile patient lifts contain actuators with an internal component that may not be strong enough to safely hold the load. In the worst case, this could cause the lifting arm to suddenly drop uncontrolled. This affects 119 units with specific serial numbers manufactured in certain batches.
- Check if your Arjo Tenor lift (Model KHA1000 US or KHA1010 US) serial number matches the recalled list
- Stop using the device immediately if your serial number is affected
- Contact Arjo customer service or your equipment supplier for instructions on inspection, repair, or replacement
- Do not attempt to repair or modify the lift yourself
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.
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1811-2026Don't want to check this manually?
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