--- title: "Siemens AG/Siemens Healthcare GmbH Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Siemens AG/Siemens Healthcare GmbH recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/siemens-ag-siemens-healthcare-gmbh/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Siemens AG/Siemens Healthcare GmbH recall records **3** reported ongoing 3 records in this archive. Latest source date Jun 26, 2024. 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 Jun 26, 2024 FDA device enforcement ### [ARTIS is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and...](https://isitonrecall.com/recall/fda-device-z-2240-2024-artis-is-a-family-of-dedicated-angiography-systems-developed-for-single-and-biplane-diagnostic-imagi/) A potential issue with ARTIS icono systems equipped with a small detector and a corresponding collimator (model # 10843101) was identified. In very rare situations, the first x-ray release following patient registration may be performed with incorrect coppe... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of TX, MA, NH, MN, OK, NJ, SC, NY, MI, IL, MO, NC. [Official source for ARTIS is a family of dedicated angiography systems developed for single and biplane diagnostic im...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2240-2024%22) Jun 26, 2024 FDA device enforcement ### [ARTIS is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and...](https://isitonrecall.com/recall/fda-device-z-2241-2024-artis-is-a-family-of-dedicated-angiography-systems-developed-for-single-and-biplane-diagnostic-imagi/) A potential issue with ARTIS icono systems equipped with a small detector and a corresponding collimator (model # 10843101) was identified. In very rare situations, the first x-ray release following patient registration may be performed with incorrect coppe... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of TX, MA, NH, MN, OK, NJ, SC, NY, MI, IL, MO, NC. [Official source for ARTIS is a family of dedicated angiography systems developed for single and biplane diagnostic im...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2241-2024%22) Jun 26, 2024 FDA device enforcement ### [ARTIS is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and...](https://isitonrecall.com/recall/fda-device-z-2242-2024-artis-is-a-family-of-dedicated-angiography-systems-developed-for-single-and-biplane-diagnostic-imagi/) A potential issue with ARTIS icono systems equipped with a small detector and a corresponding collimator (model # 10843101) was identified. In very rare situations, the first x-ray release following patient registration may be performed with incorrect coppe... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of TX, MA, NH, MN, OK, NJ, SC, NY, MI, IL, MO, NC. [Official source for ARTIS is a family of dedicated angiography systems developed for single and biplane diagnostic im...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2242-2024%22) ## Reasons in these listed records - A potential issue with ARTIS icono systems equipped with a small detector and a corresponding collimator (model # 10843101) was identified. In very rare situations, the first x-ray release following patient registration may be performed with incorrect copper prefiltration. If ... These examples come from this result page and are not a ranking of every recall reason. ## Checking Siemens AG/Siemens Healthcare GmbH ### Is there a recall on siemens ag/siemens healthcare gmbh right now? This archive contains 3 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 Siemens AG/Siemens Healthcare GmbH](https://isitonrecall.com/check/?q=Siemens%20AG%2FSiemens%20Healthcare%20GmbH) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)