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BD Biosciences, Systems & Reagents: Medical Device Recalls in 2015

Updated on March 25, 2026.

According to to data from the FDA, there were 5 medical device recalls made by BD Biosciences, Systems & Reagents in 2015. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.
See this for other years:
2012
2014
2015
  • BD FACSCalibur; Catalog Numbers 342973, 342975, 34976 In vitro Diagnostics Use.
  • BD Flow Cytometers; used on all BD FACSCount, BD FACSCalibur, BD FACSCanto, BD FACSCanto II, BD LSR II, BD LSRFortessa,BD FACSAria, BD FACSAria II, BD FACSAria Ill, BD lnflux, BD FACSArray,BD Pathway 855, BD Pathway 435 and all SORP instruments. BD Biosciences Flow cytometers for the enumeration of tissue and biological fluid samples such as blood and blood components.
  • CD123 (9F5) PE Catalog number 649453 Analyte Specific Reagent
  • CD8 (Leu-2a) PE (In vitro diagnostic), Catalog number 340046. Hematology: Single color direct immunofluorescence reagent for enumerating percentages of mature human suppressor/cytotoxic (CD8+) lymphocytes in erythrocyte-lysed whole blood or peripheral blood mononuclear cell suspensions.
  • Anti-Lambda APC-H7, Catalog Number 656157. Product Usage: Intended for in vitro flow cytometric immunophenotyping of hematologic disorders.
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