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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

710

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 201–220 of 710 recalls

Becton, Dickinson and Company, BD Biosciences: BD Multitest 6-Color TBNK with optional BD Trucount Tubes...

Due to partial label detachment on tubes. This can cause tubes to become stuck together in the pouch or cause automation errors when used with the automated loader for the wash assistant.

FDAOct 3, 2022AL, AZ, AR +40 more• Becton, Dickinson and Company, BD Biosciences

Becton, Dickinson and Company, BD Biosciences: BD Trucount Tubes (Cat. No. 340334), used for determining...

Due to partial label detachment on tubes. This can cause tubes to become stuck together in the pouch or cause automation errors when used with the automated loader for the wash assistant. Firm root cause investigation confirmed that label detachment is due to an adhesive change by a tier 2 supplier.

FDAOct 3, 2022AL, AZ, AR +40 more• Becton, Dickinson and Company, BD Biosciences

Corin Ltd Unit 1-57-8 Corinium Centre Cirencester United Kingdom: Corin METAFIX HIP STEM, SIZE 3, STANDARD, 135 degrees, CO...

One MetaFix size 7 collarless stem from batch 478179 which was incorrectly labelled as a MetaFix size 3 collared stem from batch 485630.

1...9 101112 13...36

Page 11 of 36Next

FDAJul 22, 2022Nationwide• Corin Ltd Unit 1-57-8 Corinium Centre Cirencester United Kingdom

Qiagen Sciences LLC: FGFR RGQ RT-PCR Kit (RUO, not IVD) REF 8747010

Increased occurrence rate of false positive results, lead to a false positive sample result that could subsequently be incorrectly reported from the laboratory. A false positive result could lead to the risk of the patient being exposed to an inappropriate or suboptimal anti-cancer treatment and/or unnecessarily experiencing side effects

FDAJul 20, 2022IN, MN, NC +1 more• Qiagen Sciences LLC

Qiagen Sciences LLC: therascreen FGFR RGQ RT-PCR kit (US IVD) REF 874721

FDAJul 20, 2022IN, MN, NC +1 more• Qiagen Sciences LLC

Corin Ltd Unit 1-57-8 Corinium Centre Cirencester United Kingdom: TaperFit Stem, Size 0, 38mm OFFSET, 12/14 Taper + 188.550...

Some of the devices did not pass fatigue testing.

FDAJul 12, 2022NJ• Corin Ltd Unit 1-57-8 Corinium Centre Cirencester United Kingdom

Launch Sequence Aphrodisia Capsules (Loud Muscle Science) – Unapproved Drug (2022)

Marketed Without An Approved NDA/ANDA: Unapproved Drug based on label claims.

Class IIModerate

FDAJun 27, 2022Nationwide• Loud Muscle Science

Launch Sequence Aphrodisia Capsules (Loud Muscle Science) – Undeclared Ingredient (2022)

Undeclared Allergen

Marketed Without An Approved NDA/ANDA: Product found to contain undeclared tadalafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.

Class IHigh

FDAJun 27, 2022Nationwide• Loud Muscle Science

Launch Sequence Euphoria Capsules (Loud Muscle Science) – Unapproved Drug (2022)

Marketed Without An Approved NDA/ANDA: Unapproved Drug based on label claims.

Class IIModerate

FDAJun 27, 2022Nationwide• Loud Muscle Science

Launch Sequence Capsules (Loud Muscle Science) – Undeclared Ingredient (2022)

Undeclared Allergen

Class IHigh

FDAJun 27, 2022Nationwide• Loud Muscle Science

Launch Sequence Euphoria Capsules (Loud Muscle Science) – Undeclared Ingredient (2022)

Undeclared Allergen

Class IHigh

FDAJun 27, 2022Nationwide• Loud Muscle Science

Launch Sequence Capsules (Loud Muscle Science) – Unapproved Drug (2022)

Marketed Without An Approved NDA/ANDA: Unapproved Drug based on label claims.

Class IIModerate

FDAJun 27, 2022Nationwide• Loud Muscle Science

Meridian Bioscience Inc: Revogene, Catalog no. 610210. IVD test instrument

Fire/Burn Risk

When a run is aborted, the cooling period protection does not occur and the user is able to open the lid prior to the completion of the cooling period, exposing the user to heated instrument components. Incidental contact with heated instrument components may result in an injury such as minor burns.

FDAJun 22, 2022Nationwide• Meridian Bioscience Inc

Integra LifeSciences Corp.: CereLink ICP Monitor; Catalog No. 826820, 826820P. Intra...

Integra has received complaints associated with ICP readings drifting to -50 mmHg (out-of-range) and may manifest an error message "sensor or extension cable failure!" The firm has found that this is caused by electrical interference from a component of the monitor's circuit board and from the environment.

FDAJun 22, 2022Nationwide• Integra LifeSciences Corp.

CBD Metered Dose Inhaler (Wellness BioSciences) – Unapproved Drug (2022)

Marketed Without an Approved NDA/ANDA

Class IIModerate

FDAApr 1, 2022Nationwide• Wellness BioSciences

Becton, Dickinson and Company, BD Biosciences: BD Anti-Kappa APC (Cat. No. 341098) is an analyte specifi...

Anti-Kappa APC & Anti-Kappa PE analyte reagents may exhibit uncharacteristic flow profiles.

FDAMar 25, 2022Nationwide• Becton, Dickinson and Company, BD Biosciences

Becton, Dickinson and Company, BD Biosciences: BD Anti-Kappa PE (Cat. No. 346587) is an analyte specific...

Anti-Kappa APC & Anti-Kappa PE analyte reagents may exhibit uncharacteristic flow profiles.

FDAMar 25, 2022Nationwide• Becton, Dickinson and Company, BD Biosciences

Sight Sciences, Inc.: TearCare version 1.0 SmartHubs

Ophthalmic devices distributed prior to the recently-obtained 510(k) clearance do not fall within the relevant 510(k) exemption and so their performance characteristics were not evaluated by the FDA prior to distribution.

FDAMar 23, 2022Nationwide• Sight Sciences, Inc.

Edwards Lifesciences, LLC: FORE-SIGHT ELITE Tissue Oximeter module, REF: HEMFSM10

The StO2 values may be inaccurately low when using either the FORE-SIGHT ELITE Tissue Oximeter Module or the FORE-SIGHT ELITE Absolute Tissue Oximeter Monitor with the Fore-Sight Elite large sensor in certain somatic locations (arms and legs). While the StO2 absolute values are impacted, the directional trend remains accurate, but may have a larger magnitude change. Low StO2 values may lead to unintended or inappropriate treatment

FDAMar 1, 2022Nationwide• Edwards Lifesciences, LLC

Edwards Lifesciences, LLC: FORE-SIGHT ELITE Absolute Tissue Oximeter, REF: 01-06-30...

FDAMar 1, 2022Nationwide• Edwards Lifesciences, LLC