FDA applicant

Automatic Liquid Packaging, Inc.

Woodstock, IL21 decisions1983–20000 recalls

FDA records 21 decisions for Automatic Liquid Packaging, Inc. (Woodstock, IL) from 1983 to 2000: 21 510(k) clearances. Most are in product codes CAF (Nebulizer (Direct Patient Interface)) and BTT (Humidifier, Respiratory Gas, (Direct Patient…). 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 Automatic Liquid Packaging, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Automatic Liquid Packaging, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Automatic Liquid Packaging, 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 “Automatic”

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

Automatic Medical Technologies, Inc. 2 Automatic Film Processor Corp. 1

Automatic Liquid Packaging, 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 “Automatic”