FDA applicant

Whatman Specialty Products, Inc.

Fairfield, NJ1 decision1996–19963 recalls

FDA records 1 decision for Whatman Specialty Products, Inc. (Fairfield, NJ) in 1996: 1 510(k) clearance. All are in product code PJC (Newborn Screening Specimen Collection Paper). 3 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, clinical chemistry panel, where it files most

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

FDA decisions per year

No FDA decision for Whatman Specialty Products, Inc. since 2007.

Recalls per year

3in 2009

2007high 3 (2009) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Whatman Specialty Products, 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 “Whatman”

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

Whatman, Inc. 1

Whatman Specialty Products, 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?

What has been recalled?

Other applicant names beginning “Whatman”