Becton Dickinson & Co.

Complete recall history across all FDA and CPSC categories — 183 total recalls

Becton Dickinson & Co. appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (183)

FDA medical device enforcement actions by Becton Dickinson & Co.. Showing most recent 50.

Date Product Reason Class
Oct 23, 2025 BD Kiestra" Isolate Suspension Cuvette Array; Catalog No.: 246100; The 2D barcodes on these cuvettes contain formatting errors that prevent the ... Class II
Sep 23, 2025 BD Phoenix M50 Instrument, labeled as the following: 1. BD Phoenix M50 Aut... Product service credentials used by some BD technical support teams to access... Class II
Sep 23, 2025 BD MAX System, for in vitro diagnostic (IVD) use, labeled as the following: ... Product service credentials used by some BD technical support teams to access... Class II
Sep 23, 2025 BD BACTEC Blood Culture System, labeled as the following: 1. BD BACTEC FX,... Product service credentials used by some BD technical support teams to access... Class II
Sep 23, 2025 BD Veritor Connect Software, labeled as the following: 1. Veritor (NUC), C... Product service credentials used by some BD technical support teams to access... Class II
Sep 23, 2025 BD BACTEC Blood Culture System, labeled as the following: 1. BACTEC 9120 S... Product service credentials used by some BD technical support teams to access... Class II
Sep 23, 2025 BD EpiCenter Microbiology Data Management System, labeled as the following: ... Product service credentials used by some BD technical support teams to access... Class II
Jun 23, 2025 BD COR System Software. Model Number: 444829. Potential for functionality issue that supports the Over labeling feature an... Class II
May 20, 2025 BD BACTEC" MGIT" 960 PZA Kit. IVD qualitative procedure for susceptibility te... BD has received additional complaints of intermittent false resistance result... Class II
Feb 12, 2025 BD BBL TB Stain Kit K, Catalog (REF): 212522 One component of the kit was shipped with an expiration date of 30Sep2024 whi... Class II
Dec 19, 2024 BD PCR Cartridges used with MAX System. Model Number: 437519 Potential for signal drift in specific lots of BD PCR Cartridges. Class II
Nov 6, 2024 BD BBL Sensi Disc Ampicillin 2 ¿g (AM-2) - In-Vitro BD BBL Sensi Disc Ampicil... BD identified through potency testing as part of a stability test request to ... Class II
Oct 31, 2024 BD Phoenix M50 Automated Microbiology System Version or Model: 443624 Catal... BD confirmed that product service credentials used by some BD technical suppo... Class II
Oct 31, 2024 BACTEC 9120 System Version or Model: 445570 Catalog Number: 445570 BD confirmed that product service credentials used by some BD technical suppo... Class II
Oct 31, 2024 BD BACTEC FX40 Instrument Version or Model: 442296 Catalog Number: 442296 BD confirmed that product service credentials used by some BD technical suppo... Class II
Oct 31, 2024 BD COR PX Instrument Version or Model: 443988 Catalog Number: 443988 BD confirmed that product service credentials used by some BD technical suppo... Class II
Oct 31, 2024 BD EpiCenter Data Management System Version or Model: 440887 Catalog Number... BD confirmed that product service credentials used by some BD technical suppo... Class II
Oct 31, 2024 BD COR MX Instrument Version or Model: 443989 Catalog Number: 443989 BD confirmed that product service credentials used by some BD technical suppo... Class II
Oct 31, 2024 BD EpiCenter Data Management System, Multi User Software Version or Model: 4... BD confirmed that product service credentials used by some BD technical suppo... Class II
Oct 31, 2024 BACTEC 9240 System Version or Model: 445475 Catalog Number: 445475 BD confirmed that product service credentials used by some BD technical suppo... Class II
Oct 31, 2024 BD EpiCenter Single User Software Version or Model: 441007 Catalog Number: ... BD confirmed that product service credentials used by some BD technical suppo... Class II
Oct 31, 2024 BD BACTEC FX, Instrument Top, Packaged Version or Model: 441385 Catalog Num... BD confirmed that product service credentials used by some BD technical suppo... Class II
Oct 31, 2024 BD MAX System, BD MAX Instrument Version or Model: 441916 Catalog Number: 4... BD confirmed that product service credentials used by some BD technical suppo... Class II
Oct 31, 2024 BD Synapsys Informatics Solution (Laboratory Solution) Version or Model: 444... BD confirmed that product service credentials used by some BD technical suppo... Class II
Oct 31, 2024 BD COR GX Instrument Version or Model: 443990 Catalog Number: 443990 BD confirmed that product service credentials used by some BD technical suppo... Class II
Sep 12, 2024 BD Synapsys Informatics Solution with software versions: 4.20, 4.30, 5.10, 5.... Synapsys software versions 4.20, 4.30, 5.10, 5.20, or 5.30 and utilizing the ... Class II
Aug 1, 2024 BD Phoenix 100-Intended for the rapid identification (ID) and antimicrobial s... Escherichia coli (E. coli) misidentification for clinical samples that were t... Class II
Aug 1, 2024 BD Phoenix M50 instrument -Intended for the rapid identification (ID) and ant... Escherichia coli (E. coli) misidentification for clinical samples that were t... Class II
Jul 18, 2024 BD BACTEC MGIT 960 PZA Kit)- IVD qualitative procedure for susceptibility te... May intermittently produce falsely resistant results for pyrazinamide (PZA) d... Class II
Jul 9, 2024 BD Kiestra Urine Culture Application Powered by BD Synapsys Informatics Solut... There is a potential risk that the image colony count does not adequately ref... Class II
May 7, 2024 BD SARS-CoV-2 Reagents for BD MAX" Systems. RT-PCR test to detect SARS-CoV-2 ... Assays may produce false negative results due to decreased activity of the en... Class II
Feb 29, 2024 BD Phoenix NMIC-306 Panel is a self-inoculating (when used with a BD Phoenix ... Products were found to have confirmed drug cross contamination prior to relea... Class II
Feb 29, 2024 BD Phoenix Yeast ID Panel is a self-inoculating (when used with a BD Phoenix ... Esculin, a substrate used in other panels and normally in A16 well, was foun... Class II
Jan 8, 2024 BD BBL Sensi Disc Clarithromycin- 15 ug, used for semi-quantitative in vitro ... There is a possibility of reproducibility, accuracy, and/or QC failures in an... Class II
Jan 8, 2024 BD BBL Sensi Disc Ampicillin with Sulbactam 10/10 ¿g, Catalog Number 231660... There is a possibility of reproducibility, accuracy, and/or QC failures in an... Class II
Jan 8, 2024 BD BBL Sensi Disc Doripenem- 15 ug, used for semi-quantitative in vitro susce... There is a possibility of reproducibility, accuracy, and/or QC failures in an... Class II
Jan 8, 2024 BD BBL Sensi Disc Ceftriaxone- 30 ug, used for semi-quantitative in vitro sus... There is a possibility of reproducibility, accuracy, and/or QC failures in an... Class II
Jan 8, 2024 BD BBL Sensi Disc Cefuroxime- 30 ug, used for semi-quantitative in vitro susc... There is a possibility of reproducibility, accuracy, and/or QC failures in an... Class II
Jan 8, 2024 BD BBL Sensi Disc Ampicillin - 10 ¿g, Catalog No. 230705 and 231264; 2 ¿g, Ca... There is a possibility of reproducibility, accuracy, and/or QC failures in an... Class II
Jan 8, 2024 BD BBL Sensi Disc Cefixime - 5 ug¿, used for semi-quantitative in vitro susce... There is a possibility of reproducibility, accuracy, and/or QC failures in an... Class II
Jan 8, 2024 BD BBL Sensi Disc Ofloxacin- 5 ug, used for semi-quantitative in vitro suscep... There is a possibility of reproducibility, accuracy, and/or QC failures in an... Class II
Jan 8, 2024 BD BBL Sensi Disc Ceftazidime- 30 ug, used for semi-quantitative in vitro sus... There is a possibility of reproducibility, accuracy, and/or QC failures in an... Class II
Jan 8, 2024 BD BBL Sensi Disc Sulfamethoxazole with Trimethoprim 23.75/1.25 ug, used for ... There is a possibility of reproducibility, accuracy, and/or QC failures in an... Class II
Jan 8, 2024 BD BBL Sensi Disc Augmentin - 3¿g, Catalog Number 291270¿used for semi-quanti... There is a possibility of reproducibility, accuracy, and/or QC failures in an... Class II
Jan 8, 2024 BD BBL Sensi Disc Levofloxacin- 5 ug, used for semi-quantitative in vitro sus... There is a possibility of reproducibility, accuracy, and/or QC failures in an... Class II
Jan 8, 2024 BD BBL Sensi Disc Aztreonam - 30 ug¿, used for semi-quantitative in vitro su... There is a possibility of reproducibility, accuracy, and/or QC failures in an... Class II
Jan 8, 2024 BD BBL Sensi Disc Ciprofloxacin- 5 ug, used for semi-quantitative in vitro su... There is a possibility of reproducibility, accuracy, and/or QC failures in an... Class II
Jan 8, 2024 BD BBL Sensi Disc Ertapenem- 10 ug, used for semi-quantitative in vitro susce... There is a possibility of reproducibility, accuracy, and/or QC failures in an... Class II
Jan 8, 2024 BD BBL Sensi Disc Chloramphenicol- 30 ug, used for semi-quantitative in vitro... There is a possibility of reproducibility, accuracy, and/or QC failures in an... Class II
Jan 8, 2024 BD BBL Sensi Disc Moxifloxacin- 5 ug, used for semi-quantitative in vitro sus... There is a possibility of reproducibility, accuracy, and/or QC failures in an... Class II

View all 183 device recalls →

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

Yes. You can search for any company using the firm/manufacturer pages for each category: Food Firms, Drug Firms, Device Firms, or Product Manufacturers. You can also use the search functionality on any browse page to find recalls by company name.

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