FDA applicant

Landec Corp.

Menlo Park, CA1 decision1994–19940 recalls

FDA records 1 decision for Landec Corp. (Menlo Park, CA) in 1994: 1 510(k) clearance. All are in product code LGF (Component, Cast). 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, orthopedic panel, where it files most

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

FDA decisions per year

No FDA decision for Landec Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Landec Corp.

Which product codes does it file in?

What has FDA decided for it lately?