PlainRecalls

Becton Dickinson & Co.

Compiled from official public sources by the editorial team.

185 recalls on record · Latest: May 6, 2026

Becton Dickinson & Co. Recall Insight

Becton Dickinson & Co. appears on 185 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.182% of the federal archive, a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated May 6, 2026, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 50 entries, severity tagging shows 0 critical, 42 moderate, and 8 lower-severity recalls. Affected-unit counts are disclosed on 50 of 50 entries, unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (50). The date window on this page runs from Feb 5, 2014 to Aug 28, 2019.

Manufacturer-level browsing is useful when monitoring a single firm for patterns, whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current, deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement, always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

FDA Devices Moderate Aug 28, 2019

Kit BD Max Vaginal Panel; Catalog # 443712

FDA Devices Moderate Aug 28, 2019

Kit BD Max ExK DNA 2 EU LUO; Catalog # 442820

FDA Devices Moderate Aug 28, 2019

Kit BD Max StaphSR; Catalog # 443419

FDA Devices Moderate Aug 28, 2019

Kit BD Max CT/GC/TV; Catalog # 442970

FDA Devices Moderate Aug 28, 2019

Kit BD Max Cdiff EU; Catalog # 442555

FDA Devices Moderate Aug 28, 2019

Kit BD Max GC RT PCR Assay; Catalog # 443486

FDA Devices Moderate Aug 28, 2019

Kit BD Max Enteric Parasite Panel EU; Catalog # 442960

FDA Devices Moderate Aug 28, 2019

Kit BD Max ExK DNA 2 USA; Catalog # 442819

FDA Devices Moderate Aug 28, 2019

Kit BD Max Enteric Bacterial Panel EU; Catalog # 442963

FDA Devices Moderate Aug 28, 2019

Kit BD Max MRSA XT; Catalog # 443461

FDA Devices Moderate May 22, 2019

BD Veritor System Reader -In Vitro Diagnostic for use with BD Veritor System Test Kit Devices Catalog Number: 256055

FDA Devices Moderate May 22, 2019

BD Veritor Plus Analyzer- In-Vitro Diagnostic intended to use with the BD Veritor System Test Devices. Catalog Number: 256066

FDA Devices Moderate Apr 3, 2019

BD Synapsys Laboratory Solutions Catalog Number:444150 Product Usage: BD Synapsys is a laboratory software solution providing data management a…

FDA Devices Moderate Mar 13, 2019

BD MAX Enteric Bacterial Panel -For In Vitro Diagnostic Use with the BD MAX System Catalog Number: 442963 The BD MAX Enteric Bacterial Panel perf…

FDA Devices Moderate Mar 6, 2019

Phoenix AST Indicator, Catalog Number 246004

FDA Devices Moderate Mar 6, 2019

Phoenix AP AST Indicator Bag, Catalog Number 246006

FDA Devices Moderate Mar 6, 2019

Phoenix AST-s Indicator, Catalog Number 246009

FDA Devices Moderate Dec 12, 2018

BD BBL Trypticase Soy Agar with 5% Sheep Blood, Catalog No. 221261, (non-selective, non-differential)

FDA Devices Moderate Nov 7, 2018

BD Max Instrument, Catalog Number 441916 441927 (refurbished instrument) - Product Usage: The BD MAX System, used in conjunction with appropriate ex…

FDA Devices Moderate Nov 7, 2018

BD Max Instrument Reader Spare Part, Catalog Number 8090369/443364, 44336409 (Repaired Reader spare part) - Product Usage: The BD MAX System, used i…

FDA Devices Low Oct 17, 2018

BD FocalPoint Slide Profiler and BD FocalPoint GS Review Station; Catalog Nos. 490398, 490653, 491085, 491086, 491090, 490189 The BD FocalPoint G…

FDA Devices Moderate Aug 29, 2018

BD BBL GC-Lect Agar; Cat. No. 297715 The device is a selective medium providing enhanced growth and recovery of Neisseria gonorrhoeae and better …

FDA Devices Low May 9, 2018

BD MAX DNA MMK (SPC) For Laboratory Use, catalog no. 442829

FDA Devices Low May 9, 2018

BD MAX DNA MMK Lab Use, catalog no. 442828

FDA Devices Moderate Mar 21, 2018

Difco" Agar Noble, 500g bottle Noble Agar is a solidifying agent that is essentially free of impurities. It is used in electrophoretic and nutriti…

FDA Devices Moderate Jan 31, 2018

BD MAXTM Vaginal Panel. Catalog Number(s): 443712 443710 443711 (RUO)for collection and transport of vaginal and endocervical swab specimens, in add…

FDA Devices Moderate Jan 31, 2018

BD MAX" UVE Specimen Collection Kit. Catalog Number(s): 443376 for collection and transport of vaginal and endocervical swab specimens, in addition…

FDA Devices Moderate Jan 31, 2018

BD MAX" CT/GC/TV. Catalog Number(s): 443824,442970,443590 (RUO).for collection and transport of vaginal and endocervical swab specimens, in addit…

FDA Devices Moderate Dec 13, 2017

TrypticaseTM Soy Agar with 5% Sheep Blood (TSA IITM), Catalog Number 221261 Trypticase Soy Agar with 5% or 10% Sheep Blood is used for cultivating f…

FDA Devices Low Dec 13, 2017

BD PhoenixTM AP, Catalog Number 448010 The BD Phoenix" AP instrument is designed for use with the BD Phoenix" system is intended to standardize ID b…

FDA Devices Moderate Dec 6, 2017

BD Phoenix PMIC-107, Catalog Number 448417, UDI #s (01)30382904484171, (10)7031818(17)180228(30)0025, IVD. PMIC-107 is a Gram positive AST Only pan…

FDA Devices Low May 3, 2017

BBL Trypticase Soy Agar with 5% Sheep Blood (TSA II) and Chocolate II Agar (GC II Agar with Hemoglobin and IsoVitaleX)  I Plate Product Usage: T…

FDA Devices Moderate Mar 15, 2017

EpiCenter Plus Microbiology Data Management System software version 6.20A, when used in conjunction with the MALDI BioTyper System . Product Usage…

FDA Devices Moderate Mar 8, 2017

BD AffirM VPIII Microbial Identification Test

FDA Devices Moderate Dec 28, 2016

BD SurePathTM Preservative Collection Vials, catalog numbers 490505, 490527, 491095, 491096, and 491097. SurePath¿ Preservative Fluid is designed…

FDA Devices Low Nov 2, 2016

PhoenixSpec AP Calibrator is used to calibrate the PhoenixSpec & Phoenix AP Instruments. The instruments are then used to measure the turbidity o…

FDA Devices Low Nov 2, 2016

PhoenixSpec Calibrator & Kit is used to calibrate the PhoenixSpec &#38 Phoenix AP Instruments. The instruments are then used to measure the turbidity…

FDA Devices Moderate May 4, 2016

Trypticase TM Soy Agar with 5% Sheep Blood (TSA IITM) // MacConkey II Agar Cat. Number 221291, Lot Number 6034889, Exp. Date : April 20, 2016 Prod…

FDA Devices Moderate Dec 30, 2015

Enterococcus Screen Agar QUAD Plate

FDA Devices Moderate Dec 30, 2015

Vancomycin Screen Agar

FDA Devices Moderate Jun 24, 2015

BD Viper LT System, catalog number 442839 when used in conjunction with the BD ProbeTec Chlamydia trachomatis (CT) Qx Assay (cat. #442959) and the BD…

FDA Devices Moderate Jun 17, 2015

BBL Port A Cul tubes with Swabs Sterile Pack, catalog number 221607. For patient sample collection.

FDA Devices Moderate Jun 17, 2015

BBL Port A Cul tubes, catalog number 221606. Patient sample collection tubes. BBL Port A Cul tubes, jars and vials contain a reduced transport mediu…

FDA Devices Moderate Jan 21, 2015

TrypticaseTM Soy Agar with 5% Sheep Blood (TSA IITM) // MacConkey II Agar Trypticase Soy Agar with 5% Sheep Blood is used for the growth of fastid…

FDA Devices Moderate Jan 21, 2015

Columbia Agar with 5% Sheep Blood Columbia Agar with 5% Sheep Blood is a general purpose culture medium used for the growth and recovery of fastid…

FDA Devices Moderate Jan 21, 2015

CDC Anaerobe 5% Sheep Blood Agar CDC Anaerobe 5% Sheep Blood Agar is an enriched, nonselective culture medium particularly useful or the isolation…

FDA Devices Moderate Sep 24, 2014

BD BBL Vancomycin Screen Agar Catalog number 222204 Vancomycin Screen Agar is used to test enterococci for resistance to vancomycin and to predict…

FDA Devices Moderate Sep 17, 2014

The BD MAX MRSA Assay, catalogue #442953. An automated qualitative in vitro diagnostic test for the direct detection of Methicillin-resistant Stap…

FDA Devices Low Jul 23, 2014

BBL CrystaLEAD Enteric/Nonfermentor (E/NF) Identification (ID) System, catalog number 245000. in vitro diagnostic for the identification of aerobic…

FDA Devices Moderate Feb 5, 2014

BD BACTEC FX 40 instrument, catalog number 442296, manufactured by BD Diagnostic Systems, 7 Loveton Circle, Sparks, MD 21152. The instrument is de…

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

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Data Sources

  • Source: FDA + CPSC + NHTSA - federal recall filings naming this firm. Verify with FDA, CPSC, or NHTSA directly.
  • Source: PlainRecalls Manufacturer Index - firm-level aggregation across all three federal recall feeds

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.