Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US
| Source | FDA Device Enforcement |
|---|---|
| Category | Medical Device |
| Severity | Medium |
| Status | ongoing |
| Recall date | March 10, 2026 |
| Reported | April 22, 2026 |
| Recalling firm | ARJOHUNTLEIGH POLSKA Sp. z.o.o. |
| Country / region | Poland N/A |
Hazard
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.
Affected products
- Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US
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