Medical DeviceAug 28, 2019
Becton Dickinson & Co Kit BD Max ExK TNA 2 recall — FDA Z-2327-2019
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
Class IIFDA: TerminatedBecton Dickinson & Co.
Recall history in this database
Classification mix: Class II: 121, Class III: 3.
Medical DeviceAug 28, 2019
Becton Dickinson & Co Kit BD Max ExK DNA 1 EU LUO recall — FDA Z-2324-2019
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
Class IIFDA: TerminatedBecton Dickinson & Co.
Medical DeviceAug 28, 2019
Becton Dickinson & Co Kit BD Max MRSA; Catalog # 442953 recall — FDA Z-2328-2019
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
Class IIFDA: TerminatedBecton Dickinson & Co.
Medical DeviceAug 28, 2019
Becton Dickinson & Co Kit BD Max Vaginal Panel recall — FDA Z-2336-2019
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
Class IIFDA: TerminatedBecton Dickinson & Co.
Medical DeviceAug 28, 2019
Becton Dickinson & Co Kit BD Max ExK DNA 2 EU LUO recall — FDA Z-2326-2019
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
Class IIFDA: TerminatedBecton Dickinson & Co.
Medical DeviceAug 28, 2019
Becton Dickinson & Co Kit BD Max StaphSR recall — FDA Z-2333-2019
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
Class IIFDA: TerminatedBecton Dickinson & Co.
Medical DeviceAug 28, 2019
Becton Dickinson & Co Kit BD Max CT/GC/TV recall — FDA Z-2331-2019
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
Class IIFDA: TerminatedBecton Dickinson & Co.
Medical DeviceAug 28, 2019
Becton Dickinson & Co Kit BD Max Cdiff EU recall — FDA Z-2322-2019
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
Class IIFDA: TerminatedBecton Dickinson & Co.
Medical DeviceAug 28, 2019
Becton Dickinson & Co Kit BD Max GC RT PCR Assay recall — FDA Z-2335-2019
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
Class IIFDA: TerminatedBecton Dickinson & Co.
Medical DeviceAug 28, 2019
Becton Dickinson & Co Kit BD Max Enteric Parasite Panel EU recall — FDA Z-2329-2019
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
Class IIFDA: TerminatedBecton Dickinson & Co.
Medical DeviceAug 28, 2019
Becton Dickinson & Co Kit BD Max ExK DNA 2 USA recall — FDA Z-2325-2019
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
Class IIFDA: TerminatedBecton Dickinson & Co.
Medical DeviceAug 28, 2019
Becton Dickinson & Co Kit BD Max Enteric Bacterial Panel EU recall — FDA Z-2330-2019
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
Class IIFDA: TerminatedBecton Dickinson & Co.
Medical DeviceAug 28, 2019
Becton Dickinson & Co Kit BD Max MRSA XT recall — FDA Z-2334-2019
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
Class IIFDA: TerminatedBecton Dickinson & Co.
Medical DeviceMay 22, 2019
Becton Dickinson & Co BD Veritor System Reader -In Vitro Diagnostic for use with BD Veritor recall — FDA Z-1314-2019
Background calibration has the potential to cause false positive or false negative test results. An incorrect test result with the BD Veritor System could lead to possible misdiagnosis and…
Class IIFDA: TerminatedBecton Dickinson & Co.
Medical DeviceMay 22, 2019
Becton Dickinson & Co BD Veritor Plus Analyzer- In-Vitro Diagnostic intended to use with the recall — FDA Z-1313-2019
Background calibration has the potential to cause false positive or false negative test results. An incorrect test result with the BD Veritor System could lead to possible misdiagnosis and…
Class IIFDA: TerminatedBecton Dickinson & Co.
Medical DeviceApr 3, 2019
Becton Dickinson & Co BD Synapsys Laboratory Solutions recall — FDA Z-1051-2019
BD Synapsys version 2.1 allowed the potential for a test order to be associated to an incorrect culture record.
Class IIFDA: TerminatedBecton Dickinson & Co.
Medical DeviceMar 13, 2019
Becton Dickinson & Co BD MAX Enteric Bacterial Panel -For In Vitro Diagnostic Use with the recall — FDA Z-0981-2019
False negative results with the BD MAX Extended Enteric Bacterial Panel when testing specifically for Enterotoxigenic Escherichia coli (ETEC) and Plesiomonas shigelloides targets of the BD…
Class IIFDA: TerminatedBecton Dickinson & Co.
Medical DeviceMar 6, 2019
Becton Dickinson & Co Phoenix AST Indicator, Catalog Number 246004 recall — FDA Z-0934-2019
Panels inoculated using certain lots of the indicator solution are demonstrating an increased occurrence of test aborts.
Class IIFDA: TerminatedBecton Dickinson & Co.
Medical DeviceMar 6, 2019
Becton Dickinson & Co Phoenix AP AST Indicator Bag, Catalog Number 246006 recall — FDA Z-0935-2019
Panels inoculated using certain lots of the indicator solution are demonstrating an increased occurrence of test aborts.
Class IIFDA: TerminatedBecton Dickinson & Co.
Medical DeviceMar 6, 2019
Becton Dickinson & Co Phoenix AST-s Indicator, Catalog Number 246009 recall — FDA Z-0933-2019
Panels inoculated using certain lots of the indicator solution are demonstrating an increased occurrence of test aborts.
Class IIFDA: TerminatedBecton Dickinson & Co.
Medical DeviceDec 12, 2018
Becton Dickinson & Co BD BBL Trypticase Soy Agar with 5% Sheep Blood, Catalog No. 221261 recall — FDA Z-0528-2019
a portion of a single lot was not manufactured in accordance with the internal formulation resulting in inhibited growth of Gram negative organisms.
Class IIFDA: TerminatedBecton Dickinson & Co.
Medical DeviceNov 7, 2018
Becton Dickinson & Co BD Max Instrument, Catalog Number 441916 441927 recall — FDA Z-0313-2019
A trend for false positive Candida glabrata results has been confirmed. The discrepant results impact the Candida glabrata target only, when in the presence of a Trichomonas vaginalis true…
Class IIFDA: TerminatedBecton Dickinson & Co.
Medical DeviceNov 7, 2018
Becton Dickinson & Co BD Max Instrument Reader Spare Part, Catalog Number 8090369/443364 recall — FDA Z-0312-2019
A trend for false positive Candida glabrata results has been confirmed. The discrepant results impact the Candida glabrata target only, when in the presence of a Trichomonas vaginalis true…
Class IIFDA: TerminatedBecton Dickinson & Co.
Medical DeviceOct 17, 2018
Becton Dickinson & Co BD FocalPoint Slide Profiler and BD FocalPoint GS Review Station recall — FDA Z-0081-2019
The device may not function at the lower end (<15 deg. C) of the labeled operating temperatures. The instrument returns to normal operating conditions when environmental temperatures are at…
Class IIIFDA: TerminatedBecton Dickinson & Co.
Understanding this recall history
This page summarizes recall records in which the official source identifies Becton Dickinson & Co. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.