FDA applicant

Oxoid U.S.A., Inc.

Mchenry, IL93 decisions1980–198911 recalls

FDA records 93 decisions for Oxoid U.S.A., Inc. (Mchenry, IL) from 1980 to 1989: 93 510(k) clearances. Most are in product codes JSK (Supplement, Culture Media) and JTO (Discs, Strips And Reagents, Microorganism…). 11 recalls are linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, microbiology panel, where it files most

How often FDA has decided Oxoid U.S.A., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Oxoid U.S.A., Inc. since 2007.

Recalls per year

1in 2017

2007high 4 (2014) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Oxoid U.S.A., 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 “Oxoid”

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

Oxoid, Ltd. 36 Oxoid Limited (Part of Thermo Fisher Scientific) 7

Oxoid U.S.A., 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?

What has been recalled?

Other applicant names beginning “Oxoid”