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Becton Dickinson & Company

Becton Dickinson & Company Recalls

All product recalls associated with Becton Dickinson & Company.

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Recall Summary

Total Recalls

1000

Past Year

726

Class I (Serious)

175

Most Recent

Jan 2026

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 4441–4460 of 11124 recalls

BD Microtainer PST LH Amber Tube (Becton Dickinson) – Sample Volume Risk (2019)

Damaged reservoir may lead to a decreased fill volume causing samples to be insufficient for testing and improper blood-to-additive ratio, potentially producing erroneous results.

Moderate

FDAMay 13, 2019Nationwide• Becton Dickinson & Company

BD Microtainer PST LH Tube (Becton Dickinson) – Sample Volume Risk (2019)

Damaged reservoir may lead to a decreased fill volume causing samples to be insufficient for testing and improper blood-to-additive ratio, potentially producing erroneous results.

Moderate

FDAMay 13, 2019Nationwide• Becton Dickinson & Company

Anastrozole Tablets (American Health) – Cross Contamination (2019)

GMP Deviations: Potential cross contamination due to cleaning procedure failure.

Class II

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Moderate

FDAMay 9, 2019Nationwide• American Health Packaging

Anastrozole Tablets (American Health) – Cross Contamination (2019)

GMP Deviations: Potential cross contamination due to cleaning procedure failure.

Class IIModerate

FDAMay 9, 2019Nationwide• American Health Packaging

Alaris Pump Infusion Set (Becton Dickinson) – Occlusion Potential (2019)

An incomplete occlusion can be caused by a variation in the wall thickness of the pumping segment of the affected infusion sets used with the. The issue has the potential to lead to unintended delivery of medication when the pump module is not in running status or can result in faster than expected drug delivery flow when the pump is infusing.

High

FDAMay 6, 2019Nationwide• Becton Dickinson & Company

Aution Hybrid AU-4050 (Arkray) – Patient Information Error (2019)

This correction is being initiated due to a software issue which results in the possibility of incorrect patient information being assigned to sample results when the following rare combination of three specific events were to occur: 1) No measurement results are generated due to an error by a urine sediment measurement. 2) The instrument is shutdown incorrectly. 3) An item rack is used for subsequent sample measurements.

Low

FDAMay 3, 2019Nationwide• Arkray Factory USA, Inc.