--- title: "Beckman Coulter Biomedical GmbH Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Beckman Coulter Biomedical 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/beckman-coulter-biomedical-gmbh/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Beckman Coulter Biomedical GmbH recall records **6** reported ongoing 6 records in this archive. Latest source date Apr 29, 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 Apr 29, 2026 FDA device enforcement ### [REMISOL Advance with Software Version 2.5 UDI-DI code: 15099590802073 The Normand Info REMISOL Advance Data Manager collects and manages data and workflow for 128 connections](https://isitonrecall.com/recall/fda-device-z-2834-2026-remisol-advance-with-software-version-2-5-udi-di-code-15099590802073-the-normand-info-remisol-advanc/) Due to software issues where does not handle combo assay results. The software may replace the final combo test result with one of the sub-results resulting in incorrect reporting of test outcomes. Class II Reported ongoing Distribution: U.S.: FL, GA, IL, MI, and PA O.U.S.: Belgium, France, Hungary, Poland, Taiwan (Province of China), Tunisia, United Arab Emirates, and United Kingdom of Great Britain and Norther... [Official source for REMISOL Advance with Software Version 2.5 UDI-DI code: 15099590802073 The Normand Info REMISOL Ad...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2834-2026%22) Jul 17, 2024 FDA device enforcement ### [Power Express, REF B90918](https://isitonrecall.com/recall/fda-device-z-2978-2024-power-express-ref-b90918/) The adhesive joint between the plastic socket and metal component of the Power Express Sample Holder can fail, causing the metal part to detach and enter the centrifuge. This detachment can result in damage to the centrifuge and potential destruction of the... Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Bahrain, Canada, China, Colombia, Egypt, France, Germany, Italy, Jordan, Korea, Kuwait, Lebanon, Malaysia,... [Official source for Power Express, REF B90918](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2978-2024%22) Jul 17, 2024 FDA device enforcement ### [PE Centrifuge, REF: B36365, a component of the Power Express](https://isitonrecall.com/recall/fda-device-z-2979-2024-pe-centrifuge-ref-b36365-a-component-of-the-power-express/) The adhesive joint between the plastic socket and metal component of the Power Express Sample Holder can fail, causing the metal part to detach and enter the centrifuge. This detachment can result in damage to the centrifuge and potential destruction of the... Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Bahrain, Canada, China, Colombia, Egypt, France, Germany, Italy, Jordan, Korea, Kuwait, Lebanon, Malaysia,... [Official source for PE Centrifuge, REF: B36365, a component of the Power Express](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2979-2024%22) Jul 17, 2024 FDA device enforcement ### [PE Centrifuge Temperature Controlled, REF: B36366, a component of the Power Express.](https://isitonrecall.com/recall/fda-device-z-2980-2024-pe-centrifuge-temperature-controlled-ref-b36366-a-component-of-the-power-express/) The adhesive joint between the plastic socket and metal component of the Power Express Sample Holder can fail, causing the metal part to detach and enter the centrifuge. This detachment can result in damage to the centrifuge and potential destruction of the... Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Bahrain, Canada, China, Colombia, Egypt, France, Germany, Italy, Jordan, Korea, Kuwait, Lebanon, Malaysia,... [Official source for PE Centrifuge Temperature Controlled, REF: B36366, a component of the Power Express.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2980-2024%22) Jun 2, 2023 FDA device enforcement ### [Beckman Coulter DxA Automation System, DxA 5000, REF: B87352, IVD, 200240V, 16A, 50/60HZ, RxOnly](https://isitonrecall.com/recall/fda-device-z-2144-2023-beckman-coulter-dxa-automation-system-dxa-5000-ref-b87352-ivd-200240v-16a-50-60hz-rxonly/) A software defect in the DxA Automation System may cause tests to be run on patient samples in tube types not compatible with the requested test, leading to erroneous patient results Class II Reported ongoing Distribution: US: AL CA FL IL IN KY MI MN MO NE NJ NV NY OH PA SC TX WI WV OUS: Australia, Belgium, Canada, China, Croatia, Czechia, Egypt, France, Germany, Greece, Hong Kong, Ireland, Israel... [Official source for Beckman Coulter DxA Automation System, DxA 5000, REF: B87352, IVD, 200240V, 16A, 50/60HZ, RxOnly](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2144-2023%22) Jun 2, 2023 FDA device enforcement ### [Beckman Coulter DxA Automation System, DxA 5000 Fit, REF: B87352, IVD, 200240V, 16A, 50/60HZ, RxOnly](https://isitonrecall.com/recall/fda-device-z-2145-2023-beckman-coulter-dxa-automation-system-dxa-5000-fit-ref-b87352-ivd-200240v-16a-50-60hz-rxonly/) A software defect in the DxA Automation System may cause tests to be run on patient samples in tube types not compatible with the requested test, leading to erroneous patient results Class II Reported ongoing Distribution: US: AL CA FL IL IN KY MI MN MO NE NJ NV NY OH PA SC TX WI WV OUS: Australia, Belgium, Canada, China, Croatia, Czechia, Egypt, France, Germany, Greece, Hong Kong, Ireland, Israel... [Official source for Beckman Coulter DxA Automation System, DxA 5000 Fit, REF: B87352, IVD, 200240V, 16A, 50/60HZ, RxOnly](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2145-2023%22) ## Reasons in these listed records - Due to software issues where does not handle combo assay results. The software may replace the final combo test result with one of the sub-results resulting in incorrect reporting of test outcomes. - The adhesive joint between the plastic socket and metal component of the Power Express Sample Holder can fail, causing the metal part to detach and enter the centrifuge. This detachment can result in damage to the centrifuge and potential destruction of the patient sample resu... - A software defect in the DxA Automation System may cause tests to be run on patient samples in tube types not compatible with the requested test, leading to erroneous patient results These examples come from this result page and are not a ranking of every recall reason. ## Checking Beckman Coulter Biomedical GmbH ### Is there a recall on beckman coulter biomedical gmbh right now? This archive contains 6 records, including 6 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 Beckman Coulter Biomedical GmbH](https://isitonrecall.com/check/?q=Beckman%20Coulter%20Biomedical%20GmbH) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)