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Becton, Dickinson and Company, BD Biosciences

Becton, Dickinson and Company, BD Biosciences Recalls

All product recalls associated with Becton, Dickinson and Company, BD Biosciences.

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Recall Summary

Total Recalls

950

Past Year

Class I (Serious)

Most Recent

Dec 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 161–180 of 950 recalls

CD11b APC (BD Biosciences) – cell staining quality (2023)

In vitro diagnostics product that impacts the quality of cell staining can cause low or dim fluorescence signal, which can lead to potential false negative results and misdiagnosis of hematological malignancy, delayed treatment, and the need for additional patient samples.

FDAOct 25, 2023Nationwide• Becton, Dickinson and Company, BD Biosciences

BD Alaris Pump Infusion Sets (Becton Dickinson) – DEHP Mislabeling (2023)

Affected infusion sets labeled as free of DEHP actually do contain di(2-ethylhexyl) phthalate (DEHP).

FDAOct 11, 2023Nationwide• Becton Dickinson & Company

BD Extension Sets (Becton Dickinson) – DEHP Mislabeling (2023)

Affected infusion sets labeled as free of DEHP actually do contain di(2-ethylhexyl) phthalate (DEHP).

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FDA

Oct 11, 2023

Nationwide

• Becton Dickinson & Company

BD Gravity Sets (Becton Dickinson) – DEHP Mislabeling (2023)

Affected infusion sets labeled as free of DEHP actually do contain di(2-ethylhexyl) phthalate (DEHP).

FDAOct 11, 2023Nationwide• Becton Dickinson & Company

BD Insyte IV Catheter (Becton Dickinson) – Needle Retraction Issue (2023)

Over-the-needle, intravascular catheters may have needles that do not retract properly into the barrel, which could result in contaminated needlestick injury, blood leaking from the insertion site or catheter, and repeat catheter insertion attempts, due to catheter being inadvertently removed from the insertion site.

FDAOct 4, 2023Nationwide• Becton Dickinson Infusion Therapy Systems Inc.

BACTEC Culture Vials (Becton Dickinson) – Barcode Duplication (2023)

Certain vials of the BD BACTEC" Plus Aerobic/F Culture Vials have a labeling issue where duplicate barcode sequence numbers have been identified on more than one vial.

FDASep 12, 2023Nationwide• Becton Dickinson & Co.

Commercial Clothes Dryers (Whirlpool) – Fire hazard (2023)

Fire/Burn Risk

This recall involves all ADC brand stacked commercial clothes dryers with a 30 lb. capacity and model number ADG-30X2R or ADG-30X2Ri. Both models were sold in on-premise and coin-operated configurations for multi-unit housing, laundromats, and other facilities that use commercial laundry equipment. Logos and branding may appear differently depending on when the unit was manufactured. The model number for each unit is printed inside near the hinges of the upper door. The ADG-30X2R units were also sold in custom colors other than white to fit location branding.

CPSCSep 7, 2023Nationwide• Whirlpool Corporation, of Benton Harbor, Michigan

BD Cathena Safety IV Catheter (Becton Dickinson) – shield engagement problem (2023)

There is the potential that the safety shield may not properly engage on IV catheters. The needle can pull through the safety shield and disconnect from the needle safety shield leaving the contaminated needle point exposed.

FDAAug 29, 2023Nationwide• Becton Dickinson Infusion Therapy Systems Inc.

MINISCAV Vacuum Pump (RA Medical) – documentation inadequacy (2023)

Inadequate documentation of acceptance activity

FDAAug 23, 2023OH• R A Medical Services Holmes House Skipton Road Keighley United Kingdom

Amana PTAC Air Conditioners (Daikin) – Potential module issue (2023)

Fire/Burn Risk

This recall involves Amana-branded Packaged Terminal Air Conditioners and Heat Pumps (PTACs) assembled with "DigiAir" modules. DigiAir modules are factory-installed make-up air systems with configurable dehumidification. The recalled units are beige and have a model number that begins with PMH or PMC. Amana is printed on the unit's control cover and the model number is on the label located below the control board.

CPSCAug 3, 2023Nationwide• Daikin Comfort Technologies Manufacturing L.P. (DCT), of Houston, Texas

O-arm O2 Imaging System (Medtronic) – ground cable problem (2023)

Ground cable installed incorrectly.

FDAJul 25, 2023Nationwide• Medtronic Navigation, Inc.-Littleton

Keystone Bosworth Copaliner Varnish (Keystone) – Packaging Error (2023)

A bottle of Copaliner Solvent was inadvertently packaged into a box labeled as Copaliner Varnish (0921526) and sold as Copaliner Varnish (0921526).

FDAJul 21, 2023Nationwide• Keystone Industries

Zephyrhills Spring Water (Blue Triton) – Bromate Contamination (2023)

Bromate in finished product exceeds the MCL of 10ppb.

Class IIILow

FDAJul 14, 2023Nationwide• BLUE TRITON

Iron Dietary Supplements (Prodigy) – Packaging issue (2023)

This recall involves Ferrous Sulfate Enteric-Coated Tablets dietary supplements containing 324 mg of ferrous sulfate (iron) in bottles of 100 tablets. "Nationwide Pharmaceutical" and its logo are printed on the top left of the bottle's label panel. The recalled bottles include lot numbers M0786, M0816, M0817 and M0818, which are printed on the bottom of the bottle.

CPSCJun 22, 2023Nationwide• Prodigy Innovation LLC, of Princeton, New Jersey

Snack Tray (Wegmans) – Undeclared Allergens (2023)

Undeclared Gluten

Undeclared almonds and/or undeclared wheat

Class IIModerate

FDAJun 15, 2023IN, NY, PA• Stellex/CF Houston, LLC

Snack Tray (Wegmans) – Undeclared Allergens (2023)

Undeclared Gluten

Undeclared almonds and/or undeclared wheat

Class IIModerate

FDAJun 15, 2023IN, NY, PA• Stellex/CF Houston, LLC

BD Synapsys Informatics Solution (Becton Dickinson) – Patient Data Mis-association (2023)

There is a risk of mis-association of patient demographic data for users who choose to report results manually when their Service Control Unit (SCU) is operating near capacity and are using save actions (Skip, Final Discard, Mark as Read, Save) to process patient results rapidly.

FDAJun 8, 2023CA, CO, IL +12 more• Becton Dickinson & Co.

MICRO-X Rover Mobile X-ray System (Micro-X) – Exposure Time Limitation (2023)

Shots were terminated by the mAs integrator; however, the 4 ms exposure time did not allow enough tolerance to achieve diagnostic exposures due to variations in hardware and how different timers are started.

FDAMay 31, 2023Nationwide• Micro-X Ltd. Unit 14 6 Mab Eastern Promenade Tonsley Australia

Keystone Arcadia (KEYSTONE) – Structural Cabinet Issue (2023)

Keystone RV Company (Keystone) is recalling certain 2021-2023 Arcadia travel trailers. The backer board behind the cabinet for the wardrobe may not have been installed during production.

NHTSAMay 26, 2023Nationwide• KEYSTONE

RET Proximal Probe. Used in Fluorescence in situ hybridiz... (Cytocell Ltd. 418 Cambridge Science Park, Milton Road Oxford Gene Technology Cambridge United Kingdom) – dnas used during the manufacture of t... (2023)

DNAs used during the manufacture of two affected models were accidentally inverted during manufacturing.

FDAMay 24, 2023Nationwide• Cytocell Ltd. 418 Cambridge Science Park, Milton Road Oxford Gene Technology Cambridge United Kingdom