FDA applicant

Becton Dickinson Biosciences

Sparks, MD1 decision2001–20010 recalls

FDA records 1 decision for Becton Dickinson Biosciences (Sparks, MD) in 2001: 1 510(k) clearance. All are in product code NDZ (Assay, Nucleic Acid Amplification, Growth…). 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, microbiology panel, where it files most

How often FDA has decided Becton Dickinson Biosciences’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Becton Dickinson Biosciences since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Becton Dickinson Biosciences 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 Consumer Products 3 Becton, Dickinson and Company (Bard Access Systems… 1

Becton Dickinson Biosciences

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Becton”