ARJOHUNTLEIGH POLSKA Sp. z.o.o recalls
4 official recalls and safety alerts involving ARJOHUNTLEIGH POLSKA Sp. z.o.o since 2021-10, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.
This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with ARJOHUNTLEIGH POLSKA Sp. z.o.o or the relevant agency.
- 2026-04-22
USARJOHUNTLEIGH POLSKA Sp. z.o.o. recalls Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US
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…
- 2024-01-03
- US
- 2022-06-01
- US
ARJOHUNTLEIGH POLSKA Sp. z.o.o. recalls Sara Plus Active Floor Lift
The device may emit smoke or ignite.
FDA · DeviceARJOHUNTLEIGH POLSKA Sp. z.o.o.US Nationwide and Worldwide distributionOfficial notice → - 2021-10-06
- US
ARJOHUNTLEIGH POLSKA Sp. z.o.o. recalls Arjo Citadel beds originally assembled with the IndiGo modules during manufcturing, model number CX812A3J3AMAD0; and IndiGo…
The IndiGo power cord might wear during use which could lead to its damage, resulting in the cord being cut, burnt or short circuit with limited emission of sparks.
FDA · DeviceARJOHUNTLEIGH POLSKA Sp. z.o.o.US Nationwide distribution in the states of CA, FL, IL, KY, MD, NV, NY, PA,…Official notice →