FDA applicant

Smith River Biologicals

Mchenry, IL12 decisions1984–19930 recalls

FDA records 12 decisions for Smith River Biologicals (Mchenry, IL) from 1984 to 1993: 12 510(k) clearances. Most are in product codes JSI (Culture Media, Selective And Differential) and JSD (Culture Media, Selective Broth). 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, microbiology panel, where it files most

How often FDA has decided Smith River Biologicals’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Smith River Biologicals since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Smith River Biologicals by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Smith”

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

Smith & Nephew, Inc. 556 Smith & Nephew Richards, Inc. 88 Smith & Nephew United, Inc. 34 Smith & Nephew Medical Limited 33 Smith & Nephew Dyonics, Inc. 22 Smith & Nephew Endoscopy, Inc. 18 Smith and Nephew Donjoy, Inc. 15 Smith & Nephew, Inc., Orthopaedic Div. 10 Smith & Nephew Perry 10 Smith & Nephew Inc., Endoscopy Div. 10 Smith & Nephew, Mpl Division 9 Smith and Nephew, Inc. 8

Smith River Biologicals

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Smith”