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., part of Becton DickinsonLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Becton, Dickinson and Company, BD Biosciences with 35 device recalls. The most recent is a device recall dated May 8, 2024: BD Multitest 6-Color TBNK CE-IVD, REF: 644611; BD Multitest 6-Color TBNK Kit with BD Tr….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| May 8, 2024 | BD Multitest 6-Color TBNK CE-IVD, REF: 644611; BD Multitest 6-Color TBNK Kit with BD Trucount Tubes CE-IVD, REF: 337166; BD Multitest 6-CoClass II · Multitest with compromised raw material used to assess immune system status may result in flow cytometry plot with unusu | Device recalls |
| Oct 25, 2023 | CD11b APC: ASR, REF: 340936, and CE, REF: 333143Class II · In vitro diagnostics product that impacts the quality of cell staining can cause low or dim fluorescence signal, which c | Device recalls |
| Oct 3, 2022 | BD Multitest 6-Color TBNK with optional BD Trucount Tubes (Cat. No. 662995), for use with BD FACSLyric, BD FACSCanto II, and BD FACSCanto flClass II · Due to partial label detachment on tubes. This can cause tubes to become stuck together in the pouch or cause automation | Device recalls |
| Oct 3, 2022 | BD Trucount Tubes (Cat. No. 663028), used for determining absolute counts of leukocytes in blood. BD Trucount Tubes are designed for use witClass II · Due to partial label detachment on tubes. This can cause tubes to become stuck together in the pouch or cause automation | Device recalls |
| Oct 3, 2022 | BD Trucount Tubes (Cat. No. 340334), used for determining absolute counts of leucocytes in blood. BD Trucount tubes are designed for use witClass II · Due to partial label detachment on tubes. This can cause tubes to become stuck together in the pouch or cause automation | Device recalls |
| Mar 25, 2022 | BD Anti-Kappa PE (Cat. No. 346587) is an analyte specific reagent for the Anti-Kappa antibody, which specifically recognizes the kappa lightClass II · Anti-Kappa APC & Anti-Kappa PE analyte reagents may exhibit uncharacteristic flow profiles. | Device recalls |
| Mar 25, 2022 | BD Anti-Kappa APC (Cat. No. 341098) is an analyte specific reagent for the Anti-Kappa antibody, which specifically recognizes the kappa lighClass II · Anti-Kappa APC & Anti-Kappa PE analyte reagents may exhibit uncharacteristic flow profiles. | Device recalls |
| Jul 22, 2021 | BD" Mouse IgG2a Isotype Control APC X39 ASRClass II · Complaints have been received for performance issues related to high background and staining. this issues is related to | Device recalls |
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
