Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 17 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Becton Dickinson and its 88 subsidiaries with 2,673 510(k) clearances, 1,129 device recalls, 50 drug recalls, 8 drug applications, 3 warning letters and 1 AI-enabled device. The most recent is a 510(k) clearance dated Oct 16, 2026: BD Vacutainer® Serum Blood Collection Tubes; BD Vacutainer® Rapid Serum Tubes (RST).
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, Becton Dickinson and its 88 subsidiaries
A hatched bar is a year that is not over, so its count covers only part of the year.
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
