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, 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 Feb 14, 2024 to May 6, 2026.

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 May 6, 2026

BD GasPak EZ CO2 Pouch System. Catalog Number: 260684. for microbiologic use

FDA Devices Moderate May 6, 2026

BD GasPak EZ Campy Pouch System. Catalog Number: 260685. for microbiologic use

FDA Devices Moderate Nov 19, 2025

BD Kiestra" Isolate Suspension Cuvette Array; Catalog No.: 246100;

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 Oct 29, 2025

BD MAX System, for in vitro diagnostic (IVD) use, labeled as the following: 1. BD MAX System, BD MAX Instrument, Catalog Numbers: 44191609, 441927.

FDA Devices Moderate Oct 29, 2025

BD Phoenix M50 Instrument, labeled as the following: 1. BD Phoenix M50 Automated Microbiology System, Catalog Numbers: 443624, 44362409.

FDA Devices Moderate Jul 30, 2025

BD COR System Software. Model Number: 444829.

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 Dec 11, 2024

BD EpiCenter Data Management System Version or Model: 440887 Catalog Number: 440887

FDA Devices Moderate Dec 11, 2024

BD COR PX Instrument Version or Model: 443988 Catalog Number: 443988

FDA Devices Moderate Dec 11, 2024

BD BACTEC FX40 Instrument Version or Model: 442296 Catalog Number: 442296

FDA Devices Moderate Dec 11, 2024

BD BBL Sensi Disc Ampicillin 2 ¿g (AM-2) - In-Vitro BD BBL Sensi Disc Ampicillin 2 ¿g (AM-2) are used for semi-quantitative in vitro susceptibility t…

FDA Devices Moderate Dec 11, 2024

BACTEC 9120 System Version or Model: 445570 Catalog Number: 445570

FDA Devices Moderate Dec 11, 2024

BD Phoenix M50 Automated Microbiology System Version or Model: 443624 Catalog Number: 443624

FDA Devices Moderate Oct 16, 2024

BD Synapsys Informatics Solution with software versions: 4.20, 4.30, 5.10, 5.20 and 5.30- IVD standalone laboratory software solution providing data…

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 Aug 21, 2024

BD Kiestra Urine Culture Application Powered by BD Synapsys Informatics Solution; Catalog (Ref): 444900;

FDA Devices Moderate Jun 12, 2024

BD SARS-CoV-2 Reagents for BD MAX" Systems. RT-PCR test to detect SARS-CoV-2 in nasal, nasopharyngeal, oropharyngeal swab specimens, and saliva speci…

FDA Devices Moderate Apr 10, 2024

BD Phoenix Yeast ID Panel is a self-inoculating (when used with a BD Phoenix Automated Microbiology System) polystyrene panel (tray) containing contr…

FDA Devices Moderate Apr 10, 2024

BD Phoenix NMIC-306 Panel is a self-inoculating (when used with a BD Phoenix Automated Microbiology System) polystyrene panel (tray) containing contr…

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¿

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.