FDA applicant

Douglas Products

Walker, MI1 decision1983–19830 recalls

FDA records 1 decision for Douglas Products (Walker, MI) in 1983: 1 510(k) clearance. All are in product code KFZ (Humidifier, Non-Direct Patient Interface…). 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, anesthesiology panel, where it files most

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

FDA decisions per year

No FDA decision for Douglas Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Douglas”

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

Douglas Medical Products Corp. 20 Douglas James Donaldson Compliance Services 5 Douglas Scientific Products 2 Douglas C. Yoon, Dds 1 Douglas Manufacturer Co. 1 Douglas C. Mckee & Co. 1 Douglas Bueschel 1

Douglas Products

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Douglas”