FDA applicant

Vitex

Mchenry, IL1 decision1984–19840 recalls

FDA records 1 decision for Vitex (Mchenry, IL) in 1984: 1 510(k) clearance. All are in product code JRC (Micro Pipette). No 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, clinical chemistry panel, where it files most

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

FDA decisions per year

No FDA decision for Vitex since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Vitex by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Vitex

Which product codes does it file in?

What has FDA decided for it lately?