RecallWatchUSA

Home / Brands / ARJOHUNTLEIGH POLSKA Sp. z.o.o

ARJOHUNTLEIGH POLSKA Sp. z.o.o Recalls

10 recalls on record · October 1, 2014 to April 22, 2026 · Medical Devices

Recalls by year

14
16
18
20
21
22
24
26

Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.

April 22, 2026Medical DevicesFDA
ARJOHUNTLEIGH POLSKA Sp. z.o.o. recalls Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US
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.
January 3, 2024Medical DevicesFDA
ARJOHUNTLEIGH POLSKA Sp. z.o.o. recalls Arjo medical beds, Models Enterprise 5000X, Enterprise 8000X, Enterprise 9000X and Citadel, assembled with IndiGo Drive
Hazard: Unintended movement of bed wheels
January 3, 2024Medical DevicesFDA
ARJOHUNTLEIGH POLSKA Sp. z.o.o. recalls Arjo medical beds, Models Enterprise 5000X, Enterprise 8000X, Enterprise 9000X and Citadel, assembled with IndiGo Drive
Hazard: Unintended movement of bed wheels
June 1, 2022Medical DevicesFDA
ARJOHUNTLEIGH POLSKA Sp. z.o.o. recalls Sara Plus Active Floor Lift
Hazard: The device may emit smoke or ignite.
October 6, 2021Medical DevicesFDA
ARJOHUNTLEIGH POLSKA Sp. z.o.o. recalls Arjo Citadel beds originally assembled with the IndiGo modules during manufcturing, model number CX812A3J3AMAD0; and Ind
Hazard: 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.
August 26, 2020Medical DevicesFDA
ARJOHUNTLEIGH POLSKA Sp. z.o.o. recalls Bariatric Bed Frame System The Citadel Plus Bariatric Bed Frame System is intended for the acute and post-acute care
Hazard: Modular Junction Box (MJB) cables can melt and affect the bed functionality.
March 18, 2020Medical DevicesFDA
ARJOHUNTLEIGH POLSKA Sp. z.o.o. recalls Concerto & Basic Shower Trolly, Model Numbers BAB1000-01 (UDI: (01)05055982788083), BAB1000CON6102 [(01)05056097364483]
Hazard: The firm has become aware that any of the 4 safety catches may exhibit a mechanical failure (break in one of the arms of safety catch), which in certain circumstances may contribute to the side support unintentionally opening and may lead to a potential risk of a patient fall. The patient falling could lead to various types of injuries.
December 19, 2018Medical DevicesFDA
ARJOHUNTLEIGH POLSKA Sp. z.o.o. recalls ARJOHUNTLEIGH GETINGE GROUP Flites Passive Clip Sling - Product Usage: The Arjo Passive Clip Sling is a product intend
Hazard: Inspection process at the manufacturer found nonwoven material was used in specific lots of product that may break wile in use during the patient/resident transfer. Patient/resident might fall on the floor. IN consequence, the patient might sustain a major trauma, head injury - damage to tissue that is irreversible or may lead to death.
September 14, 2016Medical DevicesFDA
ARJOHUNTLEIGH POLSKA Sp. z.o.o. recalls ArjoHuntleigh Sara Combilizer; Intended to facilitate early immobilization, rehabilitation, and care of patients.
Hazard: ArjoHuntleigh has concluded that a device tipping hazard may occur on the current Sara Combilizer lifting mechanism, providing a potential for risk to the patient or the caregiver. The tipping phenomenon has been found during internal device testing. To date, there have been no adverse events or customer complaints related to the tipping phenomenon. The tipping hazard may occur when fully loaded Sara Combilizer in "stretcher mode" is lifted to the highest position (approximately 984 mm = 38 3/4") and tilted backwards to the angle of 25 degrees¿-28 degrees¿. Although such scenario has been defined as highly unlikely to occur during use with patients, as a commitment to quality, ArjoHuntleigh is providing customers with information on action needed. The Sara Combilizer may stay in use until the upgrade will be performed, on the condition that the tilt angle in the device ''stretcher mode" will be no greater than minus 15 degrees¿ and the device is not loaded over 330 lbs (150 kg).
October 1, 2014Medical DevicesFDA
ARJOHUNTLEIGH POLSKA Sp. z.o.o. recalls Minstrel (with scale) Product Usage: is a mobile passive hoist. It is intended for lifting and transporting adult res
Hazard: ArjoHuntleigh received three reports where the bolt under the scale unscrewed from the scale. There is a remote risk concerning the bolt unscrewing from the scale. When the scale and bolt parts are not correctly serviced, or when they receive a sharp blow during or outside of use, it is possible the bolt holding the spreader bar to the scale could unscrew during subsequent use. As a result, the sp