510(k) Report

FDA applicant

Springwood Microbiologicals

Mchenry, IL2 decisions1981–19810 recalls

FDA records 2 decisions for Springwood Microbiologicals (Mchenry, IL) in 1981: 2 510(k) clearances. Most are in product codes LHL (Reagents, Antibody, Legionella, Direct &…) and GTX (Antisera, Fluorescent, All Groups…). 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 Springwood Microbiologicals’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Springwood Microbiologicals since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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