510(k) Report

FDA applicant

Biological & Diagnostic Products

Mchenry, IL1 decision1982–19820 recalls

FDA records 1 decision for Biological & Diagnostic Products (Mchenry, IL) in 1982: 1 510(k) clearance. All are in product code DON (Radioimmunoassay, Digoxin (125-I), Rabbit…). 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, clinical toxicology panel, where it files most

How often FDA has decided Biological & Diagnostic Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Biological & Diagnostic Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Biological”

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