FDA applicant

Action Manufacturing, Inc.

Marshall, MN3 decisions2018–20220 recalls

FDA records 3 decisions for Action Manufacturing, Inc. (Marshall, MN) from 2018 to 2022: 3 510(k) clearances. Most are in product codes IPL (Wheelchair, Standup) and ITI (Wheelchair, Powered). 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, physical medicine panel, where it files most

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

FDA decisions per year

1in 2022

2018high 2 (2018) · low 0 (2019)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2018.

FIG. 1 — Action Manufacturing, Inc. by year, 2018–2026Sources: 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 Products, Inc. 2 Action Eyewear Corp. 2 Action Medical Systems, Inc. 2 Action Engineering, Inc. 1 Action Hygiene Products, Inc. 1 Action Labs, Inc. 1

Action Manufacturing, 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?

Other applicant names beginning “Action”