FDA applicant

Vanguard Container Corp.

East Brunswick, NJ1 decision1995–19950 recalls

FDA records 1 decision for Vanguard Container Corp. (East Brunswick, NJ) in 1995: 1 510(k) clearance. All are in product code FMI (Needle, Hypodermic, Single Lumen). 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 Vanguard Container Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Vanguard Container Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Vanguard”

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

Vanguard Medical Concepts, Inc. 33 Vanguard Biomedical Corp. 10 Vanguard Diagnostic Systems 2

Vanguard Container Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Vanguard”