Becton Dickinson & Co. recalls

32 recalls on record · latest: April 7, 2026

Official U.S. recall history for Becton Dickinson & Co., compiled from official government records.

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Becton Dickinson & Co. recalls BD GasPak EZ Campy Pouch System. Catalog Number: 260685. for microbiologic use

April 7, 2026 · Medical device recalls Moderate risk BD identified an issue affecting certain lots of BD GasPak EZ CO2 and BD GasPak…

Becton Dickinson & Co. recalls BD GasPak EZ CO2 Pouch System. Catalog Number: 260684. for microbiologic use

April 7, 2026 · Medical device recalls Moderate risk BD identified an issue affecting certain lots of BD GasPak EZ CO2 and BD GasPak…

Becton Dickinson & Co. recalls BD Kiestra" Isolate Suspension Cuvette Array; Catalog No.: 246100;

October 23, 2025 · Medical device recalls Moderate risk The 2D barcodes on these cuvettes contain formatting errors that prevent the an…

Becton Dickinson & Co. recalls BD Phoenix M50 Instrument, labeled as the following: 1. BD Phoenix M50 Automated Microbiology System, Catalog Numbers:…

September 23, 2025 · Medical device recalls Moderate risk Product service credentials used by some BD technical support teams to access c…

Becton Dickinson & Co. recalls BD MAX System, for in vitro diagnostic (IVD) use, labeled as the following: 1. BD MAX System, BD MAX Instrument, Catalo…

September 23, 2025 · Medical device recalls Moderate risk Product service credentials used by some BD technical support teams to access c…

Becton Dickinson & Co. recalls BD BACTEC Blood Culture System, labeled as the following: 1. BD BACTEC FX, Instrument Top, Packaged, Catalog Number: 44…

September 23, 2025 · Medical device recalls Moderate risk Product service credentials used by some BD technical support teams to access c…

Becton Dickinson & Co. recalls BD Veritor Connect Software, labeled as the following: 1. Veritor (NUC), Catalog Number: 444881. Transfers in vitro dia…

September 23, 2025 · Medical device recalls Moderate risk Product service credentials used by some BD technical support teams to access c…

Becton Dickinson & Co. recalls BD BACTEC Blood Culture System, labeled as the following: 1. BACTEC 9120 System, Catalog Numbers: 445570, 445702. 2. IN…

September 23, 2025 · Medical device recalls Moderate risk Product service credentials used by some BD technical support teams to access c…

Becton Dickinson & Co. recalls BD EpiCenter Microbiology Data Management System, labeled as the following: 1. Computer System Epicenter F/G, Catalog N…

September 23, 2025 · Medical device recalls Moderate risk Product service credentials used by some BD technical support teams to access c…

Becton Dickinson & Co. recalls BD COR System Software. Model Number: 444829.

June 23, 2025 · Medical device recalls Moderate risk Potential for functionality issue that supports the Over labeling feature and c…

Becton Dickinson & Co. recalls BD BACTEC MGIT 960 PZA Kit. IVD qualitative procedure for susceptibility testing of Mycobacterium tuberculosis, from cu…

May 20, 2025 · Medical device recalls Moderate risk BD has received additional complaints of intermittent false resistance results…

Becton Dickinson & Co. recalls BD BBL TB Stain Kit K, Catalog (REF): 212522

February 12, 2025 · Medical device recalls Moderate risk One component of the kit was shipped with an expiration date of 30Sep2024 while…

Becton Dickinson & Co. recalls BD PCR Cartridges used with MAX System. Model Number: 437519

December 19, 2024 · Medical device recalls Moderate risk Potential for signal drift in specific lots of BD PCR Cartridges.

Becton Dickinson & Co. recalls BD BBL Sensi Disc Ampicillin 2 ¿g (AM-2) - In-Vitro BD BBL Sensi Disc Ampicillin 2 ¿g (AM-2) are used for semi-quantita…

November 6, 2024 · Medical device recalls Moderate risk BD identified through potency testing as part of a stability test request to mo…

Becton Dickinson & Co. recalls BD Phoenix M50 Automated Microbiology System Version or Model: 443624 Catalog Number: 443624

October 31, 2024 · Medical device recalls Moderate risk BD confirmed that product service credentials used by some BD technical support…

Becton Dickinson & Co. recalls BACTEC 9120 System Version or Model: 445570 Catalog Number: 445570

October 31, 2024 · Medical device recalls Moderate risk BD confirmed that product service credentials used by some BD technical support…

Becton Dickinson & Co. recalls BD BACTEC FX40 Instrument Version or Model: 442296 Catalog Number: 442296

October 31, 2024 · Medical device recalls Moderate risk BD confirmed that product service credentials used by some BD technical support…

Becton Dickinson & Co. recalls BD COR PX Instrument Version or Model: 443988 Catalog Number: 443988

October 31, 2024 · Medical device recalls Moderate risk BD confirmed that product service credentials used by some BD technical support…

Becton Dickinson & Co. recalls BD EpiCenter Data Management System Version or Model: 440887 Catalog Number: 440887

October 31, 2024 · Medical device recalls Moderate risk BD confirmed that product service credentials used by some BD technical support…

Becton Dickinson & Co. recalls BD COR MX Instrument Version or Model: 443989 Catalog Number: 443989

October 31, 2024 · Medical device recalls Moderate risk BD confirmed that product service credentials used by some BD technical support…

Becton Dickinson & Co. recalls BACTEC 9240 System Version or Model: 445475 Catalog Number: 445475

October 31, 2024 · Medical device recalls Moderate risk BD confirmed that product service credentials used by some BD technical support…

Becton Dickinson & Co. recalls BD EpiCenter Data Management System, Multi User Software Version or Model: 440981 Catalog Number: 440981

October 31, 2024 · Medical device recalls Moderate risk BD confirmed that product service credentials used by some BD technical support…

Becton Dickinson & Co. recalls BD EpiCenter Single User Software Version or Model: 441007 Catalog Number: 441007

October 31, 2024 · Medical device recalls Moderate risk BD confirmed that product service credentials used by some BD technical support…

Becton Dickinson & Co. recalls BD BACTEC FX, Instrument Top, Packaged Version or Model: 441385 Catalog Number: 441385

October 31, 2024 · Medical device recalls Moderate risk BD confirmed that product service credentials used by some BD technical support…

Becton Dickinson & Co. recalls BD MAX System, BD MAX Instrument Version or Model: 441916 Catalog Number: 441916

October 31, 2024 · Medical device recalls Moderate risk BD confirmed that product service credentials used by some BD technical support…

Becton Dickinson & Co. recalls BD Synapsys Informatics Solution (Laboratory Solution) Version or Model: 444150 Catalog Number: 444150

October 31, 2024 · Medical device recalls Moderate risk BD confirmed that product service credentials used by some BD technical support…

Becton Dickinson & Co. recalls BD COR GX Instrument Version or Model: 443990 Catalog Number: 443990

October 31, 2024 · Medical device recalls Moderate risk BD confirmed that product service credentials used by some BD technical support…

Becton Dickinson & Co. recalls BD Synapsys Informatics Solution with software versions: 4.20, 4.30, 5.10, 5.20 and 5.30- IVD standalone laboratory sof…

September 12, 2024 · Medical device recalls Moderate risk Synapsys software versions 4.20, 4.30, 5.10, 5.20, or 5.30 and utilizing the in…

Becton Dickinson & product recalled over E. coli risk

August 1, 2024 · Medical device recalls Moderate risk Escherichia coli (E. coli) misidentification for clinical samples that were tes…

Becton Dickinson & product recalled over E. coli risk

August 1, 2024 · Medical device recalls Moderate risk Escherichia coli (E. coli) misidentification for clinical samples that were tes…

Becton Dickinson & Co. recalls BD BACTEC MGIT 960 PZA Kit)- IVD qualitative procedure for susceptibility testing of Mycobacterium tuberculosis, from c…

July 18, 2024 · Medical device recalls Moderate risk May intermittently produce falsely resistant results for pyrazinamide (PZA) dur…

Becton Dickinson & Co. recalls BD Kiestra Urine Culture Application Powered by BD Synapsys Informatics Solution; Catalog (Ref): 444900;

July 9, 2024 · Medical device recalls Moderate risk There is a potential risk that the image colony count does not adequately refle…