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Becton Dickinson & Recalls
364 recalls on record · July 25, 2012 to June 10, 2026 · Drugs, Medical Devices
Recalls by year
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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.
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The recall feeds record what looks like the same company under more than one name:
August 28, 2019Medical DevicesFDA
Becton Dickinson & Co. recalls Kit EXT Enteric Bacterial Panel; Catalog # 443812
Hazard: The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
August 28, 2019Medical DevicesFDA
Becton Dickinson & Co. recalls Kit BD Max Enteric Viral Panel RUO; Catalog # 443715
Hazard: The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
August 28, 2019Medical DevicesFDA
Becton Dickinson & Co. recalls Kit BD Max Vaginal Panel; Catalog # 443712
Hazard: The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
August 28, 2019Medical DevicesFDA
Becton Dickinson & Co. recalls Kit BD Max GC RT PCR Assay; Catalog # 443486
Hazard: The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
August 28, 2019Medical DevicesFDA
Becton Dickinson & Co. recalls Kit BD Max MRSA XT; Catalog # 443461
Hazard: The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
August 28, 2019Medical DevicesFDA
Becton Dickinson & Co. recalls Kit BD Max StaphSR; Catalog # 443419
Hazard: The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
August 28, 2019Medical DevicesFDA
Becton Dickinson & Co. recalls Kit BD Max StaphSR; Catalog # 443418
Hazard: The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
August 28, 2019Medical DevicesFDA
Becton Dickinson & Co. recalls Kit BD Max CT/GC/TV; Catalog # 442970
Hazard: The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
August 28, 2019Medical DevicesFDA
Becton Dickinson & Co. recalls Kit BD Max Enteric Bacterial Panel EU; Catalog # 442963
Hazard: The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
August 28, 2019Medical DevicesFDA
Becton Dickinson & Co. recalls Kit BD Max Enteric Parasite Panel EU; Catalog # 442960
Hazard: The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
August 28, 2019Medical DevicesFDA
Becton Dickinson & Co. recalls Kit BD Max MRSA; Catalog # 442953
Hazard: The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
August 28, 2019Medical DevicesFDA
Becton Dickinson & Co. recalls Kit BD Max ExK TNA 2; Catalog # 442825
Hazard: The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
August 28, 2019Medical DevicesFDA
Becton Dickinson & Co. recalls Kit BD Max ExK DNA 2 EU LUO; Catalog # 442820
Hazard: The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
August 28, 2019Medical DevicesFDA
Becton Dickinson & Co. recalls Kit BD Max ExK DNA 2 USA; Catalog # 442819
Hazard: The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
August 28, 2019Medical DevicesFDA
Becton Dickinson & Co. recalls Kit BD Max ExK DNA 1 EU LUO; Catalog # 442818
Hazard: The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
August 28, 2019Medical DevicesFDA
Becton Dickinson & Co. recalls Kit BD Max ExK DNA 1 USA; Catalog # 442817
Hazard: The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
August 28, 2019Medical DevicesFDA
Becton Dickinson & Co. recalls Kit BD Max Cdiff EU; Catalog # 442555
Hazard: The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
August 28, 2019Medical DevicesFDA
Becton Dickinson & Co. recalls Kit BD Max Check-Points CPO IVD EU; Catalog # 278102
Hazard: The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
August 28, 2019Medical DevicesFDA
Becton Dickinson & Company recalls BD Vacutainer LH (Lithium Heparin) 102 I.U. Plus Blood Collection Tubes, Catalog Number 368886
Hazard: False elevation of carboxyhemoglobin (COHb) results have been reported when using venous blood gas samples collected with tubes analyzed with the IL GEM 4000 instrument.
August 28, 2019Medical DevicesFDA
Becton Dickinson & Company recalls BD Vacutainer LH (Lithium Heparin) 68 I.U. Plus Blood Collection Tubes, Catalog Number 368884
Hazard: False elevation of carboxyhemoglobin (COHb) results have been reported when using venous blood gas samples collected with tubes analyzed with the IL GEM 4000 instrument.
August 28, 2019Medical DevicesFDA
Becton Dickinson & Company recalls BD Vacutainer LH (Lithium Heparin) 34 I.U. Plus Blood Collection Tubes, Catalog Number 368494
Hazard: False elevation of carboxyhemoglobin (COHb) results have been reported when using venous blood gas samples collected with tubes analyzed with the IL GEM 4000 instrument.
August 28, 2019Medical DevicesFDA
Becton Dickinson & Company recalls BD Vacutainer PST Gel and Lithium HeparinN (LH) 56 Units Blood Collection Tubes, Catalog Number 368056
Hazard: False elevation of carboxyhemoglobin (COHb) results have been reported when using venous blood gas samples collected with tubes analyzed with the IL GEM 4000 instrument.
August 28, 2019Medical DevicesFDA
Becton Dickinson & Company recalls BD Vacutainer PST Blood Collection Tubes, Catalog Number 368035, 368036
Hazard: False elevation of carboxyhemoglobin (COHb) results have been reported when using venous blood gas samples collected with tubes analyzed with the IL GEM 4000 instrument.
August 28, 2019Medical DevicesFDA
Becton Dickinson & Company recalls BD Vacutainer PST Gel and Lithium HeparinN (LH) 126 Units Blood Collection Tubes, Catalog Number 367964
Hazard: False elevation of carboxyhemoglobin (COHb) results have been reported when using venous blood gas samples collected with tubes analyzed with the IL GEM 4000 instrument.
August 28, 2019Medical DevicesFDA
Becton Dickinson & Company recalls BD Vacutainer PST Gel and Lithium HeparinN (LH) Blood Collection Tubes, Catalog Number 367963
Hazard: False elevation of carboxyhemoglobin (COHb) results have been reported when using venous blood gas samples collected with tubes analyzed with the IL GEM 4000 instrument.
August 28, 2019Medical DevicesFDA
Becton Dickinson & Company recalls BD Vacutainer PST Gel and Lithium HeparinN (LH) 83 Units Blood Collection Tubes, Catalog Number 367962
Hazard: False elevation of carboxyhemoglobin (COHb) results have been reported when using venous blood gas samples collected with tubes analyzed with the IL GEM 4000 instrument.
August 28, 2019Medical DevicesFDA
Becton Dickinson & Company recalls BD Vacutainer PST Gel and Lithium HeparinN (LH) 65 Units Blood Collection Tubes, Catalog Number 367961
Hazard: False elevation of carboxyhemoglobin (COHb) results have been reported when using venous blood gas samples collected with tubes analyzed with the IL GEM 4000 instrument.
August 28, 2019Medical DevicesFDA
Becton Dickinson & Company recalls BD Vacutainer PST Gel and Lithium HeparinN (LH) 56 Units Blood Collection Tubes, Catalog Number 367960
Hazard: False elevation of carboxyhemoglobin (COHb) results have been reported when using venous blood gas samples collected with tubes analyzed with the IL GEM 4000 instrument.
August 28, 2019Medical DevicesFDA
Becton Dickinson & Company recalls BD Vacutainer Lithium HeparinN (LH) 95 USP Units Blood Collection Tubes, Catalog Number 367886
Hazard: False elevation of carboxyhemoglobin (COHb) results have been reported when using venous blood gas samples collected with tubes analyzed with the IL GEM 4000 instrument.
August 28, 2019Medical DevicesFDA
Becton Dickinson & Company recalls BD Vacutainer Lithium HeparinN 75 USP Units Blood Collection Tubes, Catalog Number 367884
Hazard: False elevation of carboxyhemoglobin (COHb) results have been reported when using venous blood gas samples collected with tubes analyzed with the IL GEM 4000 instrument.