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.

Class I

Recalling firm: Omnicell, Inc.
Reason for recall: Potential for mislabeled syringe produced by the i.v.STATION device.
Affected products (lot / model / serial): 1. Part Number 258920028, Lot Number: QN 200023473. 2. Part Number 258900029, Lot Number: QN 200023474.
Units affected: 220 units
Distribution pattern: US Distribution in Alabama, Maryland and Pennsylvania.
Firm location: Cranberry Township, PA, United States
Recall type: Voluntary: Firm initiated
How the firm notified customers: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Product type: Devices
Status: Ongoing
Recall number: Z-2047-2026
Recall initiated: March 25, 2026
FDA classification date: May 13, 2026
FDA report date: May 20, 2026
FDA event ID: 98717
Last updated on HTM Vibe: July 24, 2026