FDA applicant

Martell Medical Products, Inc.

Mchenry, IL7 decisions1981–19951 recall

FDA records 7 decisions for Martell Medical Products, Inc. (Mchenry, IL) from 1981 to 1995: 7 510(k) clearances. Most are in product codes FMF (Syringe, Piston) and CBT (Arterial Blood Sampling Kit). 1 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, general hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Martell Medical Products, Inc. since 2007.

Recalls per year

1in 2022

2007high 1 (2022) · low 0 (2007)2026

Class I Class II/III not classified

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

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Martell Medical Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

What has been recalled?