Becton, Dickinson And Company, Bd Biosciences
155 North McCarthy Boulevard, Milpitas, CA, US
Registered product codes
15 product codes
Recent MDR events
1,590 on file
- BD FACSCANTO¿ II FLOW CYTOMETERJun 16, 2026Injury3027394506-2026-00005
- BD FACSLYRIC¿Feb 20, 2026Malfunction3027394506-2026-00004
- BD FACS¿ SAMPLE PREP ASSISTANT IIIFeb 6, 2026Malfunction3027394506-2026-00002
- BD FACSCANTO¿ II FLOW CYTOMETERFeb 6, 2026Injury3027394506-2026-00003
- BD FACSLYRIC¿ CEIVDFeb 5, 2026Malfunction3027394506-2026-00001
- BD FACS¿ SAMPLE PREP ASSISTANT IIIDec 12, 2025Injury3027394506-2025-00048
- BD FACSCANTO¿ II FLOW CYTOMETERDec 11, 2025Malfunction3027394506-2025-00047
- BD FACSLYRIC¿Dec 3, 2025Malfunction3027394506-2025-00046
- BD FACSLYRIC¿Nov 14, 2025Malfunction3027394506-2025-00045
- BD FACSLYRIC¿Oct 15, 2025Malfunction3027394506-2025-00044
Recalls
35 on file
- Open, ClassifiedJul 12, 2024
Multitest with compromised raw material used to assess immune system status may result in flow cytometry plot with unusual staining pattern, nonspecific aggregates, high background, double positive event increase on CD3+CD4+vsCD3+CD8+ and/or CD3-CD16+CD56+vsCD3-CD19+, contaminated antibodies, may lead to erroneous or delayed results, additional patient sample, might impact healthcare decisions
View FDA record ↗ - Open, ClassifiedJan 5, 2024
In vitro diagnostics product that impacts the quality of cell staining can cause low or dim fluorescence signal, which can lead to potential false negative results and misdiagnosis of hematological malignancy, delayed treatment, and the need for additional patient samples.
View FDA record ↗ - Open, ClassifiedNov 3, 2022
Due to partial label detachment on tubes. This can cause tubes to become stuck together in the pouch or cause automation errors when used with the automated loader for the wash assistant. Firm root cause investigation confirmed that label detachment is due to an adhesive change by a tier 2 supplier.
View FDA record ↗ - Open, ClassifiedNov 3, 2022
Due to partial label detachment on tubes. This can cause tubes to become stuck together in the pouch or cause automation errors when used with the automated loader for the wash assistant. Firm root cause investigation confirmed that label detachment is due to an adhesive change by a tier 2 supplier.
View FDA record ↗ - Open, ClassifiedNov 3, 2022
Due to partial label detachment on tubes. This can cause tubes to become stuck together in the pouch or cause automation errors when used with the automated loader for the wash assistant.
View FDA record ↗ - TerminatedMay 13, 2020
False positive reaction on the reagent.
View FDA record ↗ - TerminatedFeb 1, 2019
A customer site was identified to have three FACSLyric IVD systems with FACSuite clinical v1.1.1 installed on a computer workstation with windows 10 operating system (OS). Windows 10 OS is not a released configuration for clinical use. It is released for research use only.
View FDA record ↗ - TerminatedJul 13, 2018
The solenoid plunger tip length is too short resulting in insufficient engagement to the Universal Loader enclosure to lock during use.
View FDA record ↗ - TerminatedAug 9, 2016
Internal review found that some vials of CD3/CD4/CD45 state that the product contains gelatin. The product does not contain gelatin and should state in buffer.
View FDA record ↗ - TerminatedJan 11, 2016
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%.
View FDA record ↗
Compliance history
Matched by FEI 3027394506.
FDA inspections
0 on file
No inspections on file for this FEI number.
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.