Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Tenor is a mobile passive lift Recalled by ARJOHUNTLEIGH POLSKA SP. ZO.O. Due to ArjoHuntleigh received reports where the Tenor Lift without...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact ARJOHUNTLEIGH POLSKA SP. ZO.O. directly.
Affected Products
Tenor is a mobile passive lift, intended to be used on horizontal surfaces for lifting and transfer in hospitals, nursing homes or other healthcare facilities. Transfers with the Tenor are made indoors in the patient's room, in communal areas or in a bathroom. Tenor is meant to be used with the patient type who: sits in a wheelchair, has no capability to support themselves at all, cannot stand unsupported and is not able to bear weight (not even partially), is dependent on caregiver in most situations, is a passive resident, might be almost completely bed ridden, is often stiff and has contracted joints, and/or is totally dependent. The Tenor has a safe working load of 320 KG (705 lbs).
Quantity: 382 lifts total worldwide (160 US)
Why Was This Recalled?
ArjoHuntleigh received reports where the Tenor Lift without Scale (spreader bar) bolt broke during use. There is a remote risk concerning the breakage of the spreader bar bolt connection, part # TEN.018. During use, the bolt is subjected to mechanical forces, which may lead to breakage.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About ARJOHUNTLEIGH POLSKA SP. ZO.O.
ARJOHUNTLEIGH POLSKA SP. ZO.O. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report