FDA applicant

Whittaker General Medical

Richmond, VA1 decision1985–19850 recalls

FDA records 1 decision for Whittaker General Medical (Richmond, VA) in 1985: 1 510(k) clearance. All are in product code JPI (Device, Hematocrit Measuring). 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 Whittaker General Medical’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Whittaker General Medical since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Whittaker”

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

Whittaker Bioproducts, Inc. 30

Whittaker General Medical

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Whittaker”