--- title: "OmniCell, Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search OmniCell, 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/omnicell-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # OmniCell, Inc. recall records **3** reported ongoing 3 records in this archive. Latest source date Mar 25, 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 25, 2026 FDA device enforcement ### [Rolls of label stock used with the Omnicell i.v.Station. 1. Part Number 258920028, LABEL, STERILE, IVSTATION SYRINGE (40MMX40MM). 2. Part Number 258900029, LABEL, STERILE, IVSTA...](https://isitonrecall.com/recall/fda-device-z-2047-2026-rolls-of-label-stock-used-with-the-omnicell-i-v-station-1-part-number-258920028-label-sterile-ivstat/) Potential for mislabeled syringe produced by the i.v.STATION device. Class I Reported ongoing Distribution: US Distribution in Alabama, Maryland and Pennsylvania. [Official source for Rolls of label stock used with the Omnicell i.v.Station. 1. Part Number 258920028, LABEL, STERILE...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2047-2026%22) Feb 20, 2025 FDA device enforcement ### [IVX Station Reconstitution Transfer Set. Model Number: 298921215. Packaging: 1 set per White Tyvek Pouch, 5 Tyvek Pouches per shelf box, 10 shelf boxes per case box. IVX Station...](https://isitonrecall.com/recall/fda-device-z-1532-2025-ivx-station-reconstitution-transfer-set-model-number-298921215-packaging-1-set-per-white-tyvek-pouch/) IVX Station Reconstitution Transfer Sets were shipped in advance of the IVX Station upgrade and not intended for clinical use but are engineering devices intended for use during set up and system calibration. The items were not shipped in a validated packin... Class II Reported ongoing Distribution: Distributed in the US to Alabama [Official source for IVX Station Reconstitution Transfer Set. Model Number: 298921215. Packaging: 1 set per White Tyve...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1532-2025%22) Mar 27, 2023 FDA device enforcement ### [Omnicell IVX Station-For use in the automated preparation of pharmaceutical admixtures and syringes Model Number: 298921373](https://isitonrecall.com/recall/fda-device-z-1617-2023-omnicell-ivx-station-for-use-in-the-automated-preparation-of-pharmaceutical-admixtures-and-syringes/) IVX Station does not account for inherent scale inaccuracy or variability, could result in a preparation being passed that is outside of the dose accuracy stated in the product labeling Class II Reported ongoing Distribution: AL, NY [Official source for Omnicell IVX Station-For use in the automated preparation of pharmaceutical admixtures and syring...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1617-2023%22) ## Reasons in these listed records - Potential for mislabeled syringe produced by the i.v.STATION device. - IVX Station Reconstitution Transfer Sets were shipped in advance of the IVX Station upgrade and not intended for clinical use but are engineering devices intended for use during set up and system calibration. The items were not shipped in a validated packing configuration and ... - IVX Station does not account for inherent scale inaccuracy or variability, could result in a preparation being passed that is outside of the dose accuracy stated in the product labeling These examples come from this result page and are not a ranking of every recall reason. ## Checking OmniCell, Inc. ### Is there a recall on omnicell, inc. 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 OmniCell, Inc.](https://isitonrecall.com/check/?q=OmniCell%2C%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)