FDA applicant

Action Labs, Inc.

Independence, MO1 decision1993–19930 recalls

FDA records 1 decision for Action Labs, Inc. (Independence, MO) in 1993: 1 510(k) clearance. All are in product code ESD (Hearing Aid, Air-Conduction, Prescription). 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, ear, nose and throat panel, where it files most

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

FDA decisions per year

No FDA decision for Action Labs, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Action”

FDA records each applicant name separately; these may or may not be the same firm.

Action Manufacturing, Inc. 3 Action Products, Inc. 2 Action Eyewear Corp. 2 Action Medical Systems, Inc. 2 Action Engineering, Inc. 1 Action Hygiene Products, Inc. 1

Action Labs, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Action”