FDA applicant

Action Products, Inc.

Mchenry, IL2 decisions1980–19812 recalls

FDA records 2 decisions for Action Products, Inc. (Mchenry, IL) from 1980 to 1981: 2 510(k) clearances. Most are in product codes FMP (Protector, Skin Pressure) and JAD (System, Therapeutic, X-Ray). 2 recalls are 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 Action Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

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

Recalls per year

2in 2009

2007high 2 (2009) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Action Products, 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 Eyewear Corp. 2 Action Medical Systems, Inc. 2 Action Engineering, Inc. 1 Action Hygiene Products, Inc. 1 Action Labs, Inc. 1

Action Products, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Action”