--- title: "ARJOHUNTLEIGH POLSKA Sp. z.o.o. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search ARJOHUNTLEIGH POLSKA Sp. z.o.o. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/arjohuntleigh-polska-sp-z-o-o/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # ARJOHUNTLEIGH POLSKA Sp. z.o.o. recall records **3** reported ongoing 4 records in this archive. Latest source date Mar 10, 2026. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Mar 10, 2026 FDA device enforcement ### [Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US](https://isitonrecall.com/recall/fda-device-z-1811-2026-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 load, leading to rapid and uncontrolled... Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1811-2026%22) Aug 29, 2023 FDA device enforcement ### [Arjo medical beds, Models Enterprise 5000X, Enterprise 8000X, Enterprise 9000X and Citadel, assembled with IndiGo Drive Assistance module and retrofitted with IndiGo Drive Assis...](https://isitonrecall.com/recall/fda-device-z-0611-2024-arjo-medical-beds-models-enterprise-5000x-enterprise-8000x-enterprise-9000x-and-citadel-assembled-wi/) Unintended movement of bed wheels Class II Reported ongoing Distribution: US: TN, CA, NY, IL, NV, PA, SD [Official source for Arjo medical beds, Models Enterprise 5000X, Enterprise 8000X, Enterprise 9000X and Citadel, assem...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0611-2024%22) Aug 29, 2023 FDA device enforcement ### [Arjo medical beds, Models Enterprise 5000X, Enterprise 8000X, Enterprise 9000X and Citadel, assembled with IndiGo Drive Assistance module and retrofitted with IndiGo Drive Assis...](https://isitonrecall.com/recall/fda-device-z-0612-2024-arjo-medical-beds-models-enterprise-5000x-enterprise-8000x-enterprise-9000x-and-citadel-assembled-wi/) Unintended movement of bed wheels Class II Reported ongoing Distribution: US: TN, CA, NY, IL, NV, PA, SD [Official source for Arjo medical beds, Models Enterprise 5000X, Enterprise 8000X, Enterprise 9000X and Citadel, assem...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0612-2024%22) Apr 5, 2022 FDA device enforcement ### [Sara Plus Active Floor Lift](https://isitonrecall.com/recall/fda-device-z-1098-2022-sara-plus-active-floor-lift/) The device may emit smoke or ignite. Class I Reported terminated Distribution: US Nationwide and Worldwide distribution [Official source for Sara Plus Active Floor Lift](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1098-2022%22) ## Reasons in these listed records - 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 o... - Unintended movement of bed wheels - The device may emit smoke or ignite. These examples come from this result page and are not a ranking of every recall reason. ## Checking ARJOHUNTLEIGH POLSKA Sp. z.o.o. ### Is there a recall on arjohuntleigh polska sp. z.o.o. right now? This archive contains 4 records, including 3 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search ARJOHUNTLEIGH POLSKA Sp. z.o.o.](https://isitonrecall.com/check/?q=ARJOHUNTLEIGH%20POLSKA%20Sp.%20z.o.o.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)