OmniCell, Inc.: Medical Device Recall in 2023 - (Recall #: Z-1617-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

Omnicell IVX Station-For use in the automated preparation of pharmaceutical admixtures and syringes Model Number: 298921373

Product Classification:

Class II

Date Initiated: March 27, 2023

Date Posted: May 31, 2023

Recall Number: Z-1617-2023

Event ID: 92136

Reason for Recall:

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

Status: Ongoing

Product Quantity: 6 units

Code Information:

UDI-DI: 00860006285005 Serial Numbers: IVXS000014, IVXS000015, IVXS000016, IVXS000017, IVXS000018. IVXS000019

Distribution Pattern:

AL, NY

Voluntary or Mandated:

Voluntary: Firm initiated