Every recall we track for ARJOHUNTLEIGH POLSKA Sp. z.o.o. — 8 in all — plus the complaints and injury reports the public filed about them.
Recall of Arjo Tenor mobile passive patient lifts (models KHA1000 US and KHA1010 US) due to potential actuator failure causing uncontrolled drop. Affected units have specific serial numbers.
Arjo recalls Enterprise 5000X, 8000X, 9000X and Citadel medical beds assembled with IndiGo Drive modules due to unintended wheel movement. Affected units have specific serial numbers listed in the recall notice.
Arjo recalls Enterprise 5000X, 8000X, 9000X and Citadel medical beds with IndiGo Drive modules due to unintended wheel movement. Affected units have specific serial numbers and UDI/DI codes.
ARJOHUNTLEIGH POLSKA recalls Sara Plus Active Floor Lift models due to potential fire risk from smoke emission. Affected units include HEP0001 series and HEP2001 variants sold globally. Consumers should stop using immediately.
Arjo Citadel beds made between May 2018 and February 2021 with IndiGo modules may have power cords that wear, potentially causing cuts, burns, or short circuits. Affected units include specific model numbers and retrofitted kits.
ARJOHUNTLEIGH POLSKA recalls bariatric bed frames with modular junction box cables that may melt, affecting functionality. Serial numbers P0597830 to P0610470 are affected.
ARJOHUNTLEIGH POLSKA recalls Concerto and Basic Shower Trolly models with potential safety catch failure that could cause patient falls. Affected units include specific model numbers and serial ranges. No remedy is stated in the recall notice.
Arjo recalls passive clip slings that may break during patient transfers, risking falls and serious injury. Affected units have specific model and lot numbers.
