FDA applicant

Kabi Pharmacia, Inc.

Franklin, OH2 decisions1992–19920 recalls

FDA records 2 decisions for Kabi Pharmacia, Inc. (Franklin, OH) in 1992: 2 510(k) clearances. Most are in product codes JBQ (Antithrombin Iii Quantitation) and DGC (Ige, Antigen, Antiserum, Control). 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, hematology panel, where it files most

How often FDA has decided Kabi Pharmacia, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Kabi Pharmacia, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Kabi Pharmacia, 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 “Kabi”

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

Kabi Diagnostica 2 Kabi Pharmacia Hepar, Inc. 1

Kabi Pharmacia, 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?

Other applicant names beginning “Kabi”