Official recall record
Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US
- Issuing authority
- US FDA — Medical Devices
- Alert date
- 2026-03-10
- Country of alert
- Poland
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 05055982787758
- Brand on record
- ARJOHUNTLEIGH POLSKA Sp. z.o.o.
What the authority reported
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 to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
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