FDA applicant

Garrett Medical Products

Rancho Santa Margarita, CA3 decisions1993–19940 recalls

FDA records 3 decisions for Garrett Medical Products (Rancho Santa Margarita, CA) from 1993 to 1994: 3 510(k) clearances. Most are in product codes BTR (Tube, Tracheal (W/Wo Connector)) and CBH (Device, Fixation, Tracheal Tube). 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 Garrett Medical Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Garrett Medical Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Garrett Medical 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 “Garrett”

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

Garrett-Hewitt Intl., Inc. 1

Garrett Medical Products

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Garrett”