fda_recall · device_recall · high

ARJOHUNTLEIGH POLSKA Sp. z.o.o. — Class II recall: Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US

Event date
2026-04-22 00:00:00Z
Observed
2026-07-09 22:53:03Z
Source ID
Z-1811-2026
Payload hash
9548ab797cc3863c9ea5eaec

Summary

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. Status: Ongoing.

Informational only. Not legal, financial, or medical advice.