--- title: "Unetixs Vascular, Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Unetixs Vascular, Inc. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/unetixs-vascular-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Unetixs Vascular, Inc. recall records **4** reported ongoing 4 records in this archive. Latest source date Feb 10, 2023. 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 Feb 10, 2023 FDA device enforcement ### [MultiLab Series II 2CP & 2CP Express non-invasive vascular diagnostic device, Model Number 11996-0000-01](https://isitonrecall.com/recall/fda-device-z-1193-2023-multilab-series-ii-2cp-2cp-express-non-invasive-vascular-diagnostic-device-model-number-11996-0000-0/) The current luer fittings and adaptors allow for the possibility of the air line to be misconnected to an intravenous line, which may cause an air embolism. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and Global distribution. [Official source for MultiLab Series II 2CP & 2CP Express non-invasive vascular diagnostic device, Model Number 11996-...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1193-2023%22) Feb 10, 2023 FDA device enforcement ### [MultiLab Series II LHS TI & ERGO non-invasive vascular diagnostic device, Model Number 11949-0000-01](https://isitonrecall.com/recall/fda-device-z-1194-2023-multilab-series-ii-lhs-ti-ergo-non-invasive-vascular-diagnostic-device-model-number-11949-0000-01/) The current luer fittings and adaptors allow for the possibility of the air line to be misconnected to an intravenous line, which may cause an air embolism. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and Global distribution. [Official source for MultiLab Series II LHS TI & ERGO non-invasive vascular diagnostic device, Model Number 11949-0000-01](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1194-2023%22) Feb 10, 2023 FDA device enforcement ### [MultiLab Series II ROODRA non-invasive vascular diagnostic device, Model Number 11986-0000-01](https://isitonrecall.com/recall/fda-device-z-1195-2023-multilab-series-ii-roodra-non-invasive-vascular-diagnostic-device-model-number-11986-0000-01/) The current luer fittings and adaptors allow for the possibility of the air line to be misconnected to an intravenous line, which may cause an air embolism. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and Global distribution. [Official source for MultiLab Series II ROODRA non-invasive vascular diagnostic device, Model Number 11986-0000-01](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1195-2023%22) Feb 10, 2023 FDA device enforcement ### [MultiLab Series II REVO non-invasive vascular diagnostic device, Model Number 12950-0000-01](https://isitonrecall.com/recall/fda-device-z-1196-2023-multilab-series-ii-revo-non-invasive-vascular-diagnostic-device-model-number-12950-0000-01/) The current luer fittings and adaptors allow for the possibility of the air line to be misconnected to an intravenous line, which may cause an air embolism. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and Global distribution. [Official source for MultiLab Series II REVO non-invasive vascular diagnostic device, Model Number 12950-0000-01](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1196-2023%22) ## Reasons in these listed records - The current luer fittings and adaptors allow for the possibility of the air line to be misconnected to an intravenous line, which may cause an air embolism. These examples come from this result page and are not a ranking of every recall reason. ## Checking Unetixs Vascular, Inc. ### Is there a recall on unetixs vascular, inc. right now? This archive contains 4 records, including 4 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 Unetixs Vascular, Inc.](https://isitonrecall.com/check/?q=Unetixs%20Vascular%2C%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)