510(k) Report

FDA applicant

Omnicell, Inc.

Cranberry, PA1 decision2022–20221 recall

FDA records 1 decision for Omnicell, Inc. (Cranberry, PA) in 2022: 1 510(k) clearance. All are in product code LHI (Set, I.V. Fluid Transfer). Its devices cite 1 predicate, 0 of them its own earlier devices. 1 recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general hospital panel, where it files most

How often FDA has decided Omnicell, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2022

2022: 1
2022high 1 (2022) · low 0 (2023)2026

2026 so far, outlined.

Recalls per year

1in 2025

2025: 1
2022high 1 (2025) · low 0 (2022)2026

Class I Class II/III not classified

FIG. 1 — Omnicell, Inc. by year, 2022–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • LHISet, I.V. Fluid Transfer1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K212530IVX Fluid Transfer SetOmnicell, Inc. · 20221 recall

The one decision as Omnicell, Inc. →

What has been recalled?

1 recall linked to its devices; the latest:

  • K212530IVX Station Reconstitution Transfer Set. Model Number: 298921215. Packaging: 1 set per…Feb 20, 2025Class II