# FDA recall Z-1811-2026

> **ARJOHUNTLEIGH POLSKA Sp. z.o.o.** · Class II · device recall initiated 2026-03-10.

## Product

Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US

## Reason for recall

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.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-1811-2026
- **Recalling firm:** ARJOHUNTLEIGH POLSKA Sp. z.o.o.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-03-10
- **Report date:** 2026-04-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Komorniki, N/A, Poland

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1811-2026

## Citation

> AI Analytics. FDA recall Z-1811-2026. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-1811-2026. Source: US FDA. Licensed CC0.

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