FDA applicant

Philadelphia Biologics Center

Mchenry, IL11 decisions1982–19840 recalls

FDA records 11 decisions for Philadelphia Biologics Center (Mchenry, IL) from 1982 to 1984: 11 510(k) clearances. Most are in product codes FPA (Set, Administration, Intravascular) and FMF (Syringe, Piston). 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, general hospital panel, where it files most

How often FDA has decided Philadelphia Biologics Center’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Philadelphia Biologics Center since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Philadelphia”

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

Philadelphia Medical Specialties 6

Philadelphia Biologics Center

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Philadelphia”