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Omnicell, Inc. recalls Rolls of label stock used with the Omnicell i.v.Station. 1. Part Number 258920028, LABEL, STERILE, IVSTATION SYRING
Recalled May 20, 2026 · FDA recall Z-2047-2026 · Omnicell
Hazard
Potential for mislabeled syringe produced by the i.v.STATION device. · FDA Class I
Units
220 units
Sold at
US Distribution in Alabama, Maryland and Pennsylvania.
Description
Potential for mislabeled syringe produced by the i.v.STATION device.
Product
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, IVSTATION SYRINGE (20MMX40MM). Model/Catalog Number: IVS-RBT-001. i.v.STATION is an automation device used for preparation and compounding of IV medications, which also applies labels to compounded preparations for identification and traceability.
Manufacturer(s)
Omnicell, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →