FDA applicant

Pharmacia, Inc.

Piscataway, NJ130 decisions1976–19982 recalls

FDA records 130 decisions for Pharmacia, Inc. (Piscataway, NJ) from 1976 to 1998: 129 510(k) clearances and 1 original PMA approval. Most are in product codes DHB (System, Test, Radioallergosorbent (Rast)…) and DGC (Ige, Antigen, Antiserum, Control). Its devices cite 1 predicate, 0 of them its own earlier devices. 2 recalls are linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, immunology panel, where it files most

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

FDA decisions per year

No FDA decision for Pharmacia, Inc. since 2007.

Recalls per year

1in 2019

2007high 1 (2015) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — 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 “Pharmacia”

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

Pharmacia Deltec, Inc. 43 Pharmacia & Upjohn Co. 18 Pharmacia Diagnostics, Inc. 10 Pharmacia Deutschland GmbH 10 Pharmacia Eni Diagnostics, Inc. 2 Pharmacia Iovision, Inc. 1 Pharmacia Hepar, Inc. 1 Pharmacia Fine Chemicals 1

Pharmacia, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Pharmacia”