FDA applicant

Becton Dickinson Consumer Products

Franklin Lake, NJ3 decisions1994–19980 recalls

FDA records 3 decisions for Becton Dickinson Consumer Products (Franklin Lake, NJ) from 1994 to 1998: 3 510(k) clearances. Most are in product codes FMI (Needle, Hypodermic, Single Lumen) and KGX (Tape And Bandage, Adhesive). 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 Becton Dickinson Consumer Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Becton Dickinson Consumer Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Becton Dickinson Consumer 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 “Becton”

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

Becton, Dickinson & CO 342 Becton Dickinson Infusion Therapy Systems, Inc. 36 Becton Dickinson Microbiology Systems 33 Becton Dickinson Vascular Access, Inc. 25 Becton Dickinson Immunocytometry Systems 21 Becton Dickinson Vacutainer Systems 15 Becton Dickinson Diagnostic Instrument Systems 13 Becton Dickinson Advanced Diagnostics 10 Becton, Dickinson and Company (BD) 5 Becton Dickinson Labware 3 Becton Dickinson Biosciences 1 Becton, Dickinson and Company (Bard Access Systems… 1

Becton Dickinson Consumer Products

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Becton”