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, 50 moderate, and 0 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 6, 2021 to Oct 29, 2025.

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 Oct 29, 2025

BD EpiCenter Microbiology Data Management System, labeled as the following: 1. Computer System Epicenter F/G, Catalog Number: 441002. 2. COMPUT…

FDA Devices Moderate Oct 29, 2025

BD BACTEC Blood Culture System, labeled as the following: 1. BACTEC 9120 System, Catalog Numbers: 445570, 445702. 2. INSTRUMENT BACTEC 9120 UN…

FDA Devices Moderate Oct 29, 2025

BD Veritor Connect Software, labeled as the following: 1. Veritor (NUC), Catalog Number: 444881. Transfers in vitro diagnostic results data on the…

FDA Devices Moderate Oct 29, 2025

BD BACTEC Blood Culture System, labeled as the following: 1. BD BACTEC FX, Instrument Top, Packaged, Catalog Number: 44138509. 2. Instrument To…

FDA Devices Moderate Jul 2, 2025

BD BACTEC" MGIT" 960 PZA Kit. IVD qualitative procedure for susceptibility testing of Mycobacterium tuberculosis, from culture to pyrazinamide (PZA).

FDA Devices Moderate Mar 12, 2025

BD BBL TB Stain Kit K, Catalog (REF): 212522

FDA Devices Moderate Jan 29, 2025

BD PCR Cartridges used with MAX System. Model Number: 437519

FDA Devices Moderate Dec 11, 2024

BD COR GX Instrument Version or Model: 443990 Catalog Number: 443990

FDA Devices Moderate Dec 11, 2024

BD Synapsys Informatics Solution (Laboratory Solution) Version or Model: 444150 Catalog Number: 444150

FDA Devices Moderate Dec 11, 2024

BD MAX System, BD MAX Instrument Version or Model: 441916 Catalog Number: 441916

FDA Devices Moderate Dec 11, 2024

BD BACTEC FX, Instrument Top, Packaged Version or Model: 441385 Catalog Number: 441385

FDA Devices Moderate Dec 11, 2024

BD EpiCenter Single User Software Version or Model: 441007 Catalog Number: 441007

FDA Devices Moderate Dec 11, 2024

BD EpiCenter Data Management System, Multi User Software Version or Model: 440981 Catalog Number: 440981

FDA Devices Moderate Dec 11, 2024

BACTEC 9240 System Version or Model: 445475 Catalog Number: 445475

FDA Devices Moderate Dec 11, 2024

BD COR MX Instrument Version or Model: 443989 Catalog Number: 443989

FDA Devices Moderate Oct 2, 2024

BD Phoenix M50 instrument -Intended for the rapid identification (ID) and antimicrobial susceptibility testing (AST) of clinically significant bacter…

FDA Devices Moderate Oct 2, 2024

BD Phoenix 100-Intended for the rapid identification (ID) and antimicrobial susceptibility testing (AST) of clinically significant bacteria. The BD P…

FDA Devices Moderate Aug 28, 2024

BD BACTEC MGIT 960 PZA Kit)- IVD qualitative procedure for susceptibility testing of Mycobacterium tuberculosis, from culture to pyrazinamide (PZA) …

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Piperacillin/Tazobactam- 100/10 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231691 and 231692¿

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Azithromycin -15 ¿g, Catalog Number 231682¿used for semi-quantitative in vitro susceptibility testing.

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Rifampin- 5 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231541 and 231544¿

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Cefpodoxime - 10 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231673 and 231674¿

FDA Devices Moderate Feb 14, 2024

Sensi Disc Amoxicillin with Clavulanic Acid 20/10 ¿g, Catalog No. 231628 and 231629.¿ These discs are used for semi-quantitative in vitro suscepti…

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Minocycline - 30 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231250 and 231251¿

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Cefaclor - 30 ug¿, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231653¿

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Cefotaxime - 30 ug¿, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231606 and 231607¿; 5 ug, Catalog …

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Tetracycline 30 ug,used for semi-quantitative in vitro susceptibility testing. Catalog Number 230998 and 231344¿

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Meropenem- 10 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231703 and 231704¿

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Ceftaroline - 30 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 232231¿

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Cefepime - 30 ug¿, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231696¿

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Imipenem- 10 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231644 and 231645¿

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Moxifloxacin- 5 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231758¿

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Chloramphenicol- 30 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 230733¿and 231274¿

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Ertapenem- 10 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 232174 and 232175¿

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Ciprofloxacin- 5 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231657¿and 231658¿

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Aztreonam - 30 ug¿, used for semi-quantitative in vitro susceptibility testing. Catalog Numbers 231640¿and 231641.

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Levofloxacin- 5 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231705 and 231706¿

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Augmentin - 3¿g, Catalog Number 291270¿used for semi-quantitative in vitro susceptibility testing.

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Sulfamethoxazole with Trimethoprim 23.75/1.25 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231536…

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Ceftazidime- 30 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231632¿and 231633¿

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Ofloxacin- 5 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231672¿

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Cefixime - 5 ug¿, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231664¿

FDA Devices Moderate Jul 12, 2023

BD Synapsys Informatics Solution, Catalog Number 444150

FDA Devices Moderate Jun 14, 2023

BD Veritor System for Rapid Detection of SARS-CoV-2 & Flu A+B, 30 Single Use Test Devices- Intended for the in vitro, simultaneous qualitative detec…

FDA Devices Moderate Dec 21, 2022

BBL Chocolate II Agar- IVD for the isolation and cultivation of Neisseria species. Catalog (Ref) Number: 221267

FDA Devices Moderate Nov 23, 2022

BD Phoenix PMIC/ID-107: The Phoenix PMIC/ID panel is used for the rapid identification and susceptibility of most aerobic and facultative anaerobic …

FDA Devices Moderate May 11, 2022

BD Synapsys Microbiology Informatics Solution, Catalog Number 444150, Software Version 4.10

FDA Devices Moderate Apr 14, 2021

BD BBL Martin-Lewis Agar, 100 Ea - Product Usage: used for the isolation of pathogenic Neisseria from specimens containing mixed flora of bacteria a…

FDA Devices Moderate Apr 14, 2021

BD BBL Martin-Lewis Agar 20 Ea - Product Usage: use for the isolation of pathogenic Neisseria from specimens containing mixed flora of bacteria and f…

FDA Devices Moderate Jan 6, 2021

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

Nearby Manufacturers

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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