FDA applicant

Morrison Medical Products

Libertyville, IL8 decisions1996–19960 recalls

FDA records 8 decisions for Morrison Medical Products (Libertyville, IL) in 1996: 8 510(k) clearances. All are in product code FMQ (Restraint, Protective). 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 Morrison Medical Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Morrison Medical Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Morrison”

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

Morrison Center 1

Morrison Medical Products

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Morrison”