PlainRecalls

Becton Dickinson & Co.

128 recalls on record · Latest: Oct 29, 2025

Becton Dickinson & Co. Recall Insight

Becton Dickinson & Co. appears on 128 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.152% 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 Oct 29, 2025, 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, 48 moderate, and 2 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 Jan 21, 2015 to Jan 6, 2021.

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 Jan 6, 2021

BD Phoenix PMIC/ID-108: IVD is intended for the in vitro rapid identification (ID) of gram-positive bacteria from pure culture belonging to the gene…

FDA Devices Moderate Jan 6, 2021

BD Phoenix PMIC-108: IVD is intended for the in vitro rapid identification (ID) of gram-positive bacteria from pure culture belonging to the genera …

FDA Devices Moderate Jan 6, 2021

BD Phoenix" PMIC-109: IVD is intended for the in vitro rapid identification (ID) of gram-positive bacteria from pure culture belonging to the genera…

FDA Devices Moderate Jan 6, 2021

BD Phoenix PMIC/ID-105: IVD is intended for the in vitro rapid identification (ID) of gram-positive bacteria from pure culture belonging to the gene…

FDA Devices Moderate Jan 6, 2021

BD Phoenix PMIC/ID-109: IVD is intended for the in vitro rapid identification (ID) of gram-positive bacteria from pure culture belonging to the gene…

FDA Devices Moderate Jan 6, 2021

BD Phoenix PMIC/ID-107: IVD is intended for the in vitro rapid identification (ID) of gram-positive bacteria from pure culture belonging to the gene…

FDA Devices Moderate Jan 6, 2021

BD Phoenix PMIC-110: IVD is intended for the in vitro rapid identification (ID) of gram-positive bacteria from pure culture belonging to the genera …

FDA Devices Moderate May 27, 2020

BD BBLTM Gram Crystal Violet 250mL-- IVD Primary stain for Staining Microorganisms, Catalog Number: 212525 - Product Usage: Gram Stain Kits and Reage…

FDA Devices Moderate May 27, 2020

BD BBLTM Gram Crystal Violet 3.8L-- IVD Primary stain for Staining Microorganisms, Catalog Number: 212526 - Product Usage: Gram Stain Kits and Reagen…

FDA Devices Moderate Sep 11, 2019

BD Kiestra InoqulA+ Software Version 20.3. IVD automated specimen processing Catalog Number : 447213

FDA Devices Moderate Sep 11, 2019

BD Kiestra InoqulA Software Version 20.3.IVD automated specimen processing Catalog Number: 447202

FDA Devices Moderate Aug 28, 2019

Kit BD Max Enteric Viral Panel RUO; Catalog # 443715

FDA Devices Moderate Aug 28, 2019

Kit BD Max StaphSR; Catalog # 443418

FDA Devices Moderate Aug 28, 2019

Kit BD Max ExK DNA 1 USA; Catalog # 442817

FDA Devices Moderate Aug 28, 2019

Kit EXT Enteric Bacterial Panel; Catalog # 443812

FDA Devices Moderate Aug 28, 2019

Kit BD Max Check-Points CPO IVD EU; Catalog # 278102

FDA Devices Moderate Aug 28, 2019

Kit BD Max Enteric Viral Panel EU Catalog # 443985

FDA Devices Moderate Aug 28, 2019

Kit BD Max ExK TNA 2; Catalog # 442825

FDA Devices Moderate Aug 28, 2019

Kit BD Max ExK DNA 1 EU LUO; Catalog # 442818

FDA Devices Moderate Aug 28, 2019

Kit BD Max MRSA; Catalog # 442953

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 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 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 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 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 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 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 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 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 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…

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

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Data Sources

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