FDA applicant

Microbix Biosystems, Inc.

Canada, CA7 decisions1985–19890 recalls

FDA records 7 decisions for Microbix Biosystems, Inc. (Canada, CA) from 1985 to 1989: 7 510(k) clearances. Most are in product codes GQX (Antiserum, Cf, Varicella-Zoster) and GRF (Antiserum, Cf, Rubeola). 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 Microbix Biosystems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Microbix Biosystems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Microbix Biosystems, Inc.

Which product codes does it file in?

What has FDA decided for it lately?