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Becton, Dickinson and Company, BD Biosciences Recalls
35 recalls on record · September 2, 2015 to July 24, 2024 · Medical Devices
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
January 20, 2016Medical DevicesFDA
Becton, Dickinson and Company, BD Biosciences recalls FMC7 FITC, Catalog No. 340918 Analyte Specific Reagent.
Hazard: Becton, Dickinson and Company (BD) has determined that the FMC7 FITC (ASR) is exhibiting functional degradation. The functional degradation has the effect of reducing the percent positive from 100% down to approximately 87%.
December 2, 2015Medical DevicesFDA
Becton, Dickinson and Company, BD Biosciences recalls BD CD64 APC-R700; Analyte Specific Reagent; Model 657701; Lot No. 4344945, 5037611 and 5063945. Hematology - used as
Hazard: Three lots of CD64 (MD22) are contaminated with CD4 antibody.
November 4, 2015Medical DevicesFDA
Becton, Dickinson and Company, BD Biosciences recalls BD CD3 (SK7) FITC; IVD; Catalog # 349201 and 340542 Hematology: The CD3 antibody reacts with the epsilon chain of th
Hazard: Two lots of CD3 (SK7) FITC label contains an error in the Spanish Small text.
September 30, 2015Medical DevicesFDA
Becton, Dickinson and Company, BD Biosciences recalls CD4 (SK3), FITC; Contains CD4 FITC with gelatin and 0.1% sodium Azide. Catalog number 340133 in vitro diagnostic us
Hazard: CD4 FITC label contains an error in the Spanish small text - it states CD8 FITC.
September 2, 2015Medical DevicesFDA
Becton, Dickinson and Company, BD Biosciences recalls BD CD56 PE Cy 7: NCAM16.2 ASR Analyte Specific Reagent, Catalog number 335809 Hematology: The CD 56 antigen promote
Hazard: Three lots of CD56 PE Cy 7, Catalog number 335809, contain a low amount of HLA-DR PE antibody which could result in an unexpected staining pattern.