ARJOHUNTLEIGH POLSKA Sp. z.o.o. 2026-04-22 Health serious FDA
Health · FDA · Recall #FDA-Z-1811-2026
Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US Recall
Issued April 22, 2026 · ARJOHUNTLEIGH POLSKA Sp. z.o.o.
In April 2026, ARJOHUNTLEIGH POLSKA Sp. z.o.o. recalled the Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
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.
What you should do
- 1 Stop using Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact ARJOHUNTLEIGH POLSKA Sp. z.o.o. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- ARJOHUNTLEIGH POLSKA Sp. z.o.o.
- Category
- Health
- Recall date
- April 22, 2026
- Units affected
- Not reported
- Sold at
- US Nationwide distribution.
- Recall number
- FDA-Z-1811-2026
- Made in
- Poland
- Issuing agency
- FDA
In context
- ARJOHUNTLEIGH POLSKA Sp. z.o.o. has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 356th Health recall we've logged in 2026.