FDA applicant

Carie Med-Tech Services, Inc.

Olney, IL1 decision1993–19930 recalls

FDA records 1 decision for Carie Med-Tech Services, Inc. (Olney, IL) in 1993: 1 510(k) clearance. All are in product code BYH (Drain, Tee (Water Trap)). 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 Carie Med-Tech Services, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Carie Med-Tech Services, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Carie Med-Tech Services, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Carie Med-Tech Services, Inc.

Which product codes does it file in?

What has FDA decided for it lately?