Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BD Trucount Tubes (Cat. No. 663028) Recalled by Becton, Dickinson and Company, BD Biosciences Due to Due to partial label detachment on tubes. This...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Becton, Dickinson and Company, BD Biosciences directly.
Affected Products
BD Trucount Tubes (Cat. No. 663028), used for determining absolute counts of leukocytes in blood. BD Trucount Tubes are designed for use with in vitro diagnostic products such as BD Tritest reagents, and a suitably equipped flow cytometer. BD Trucount Tubes can be used with the BD FACS Loader.
Quantity: 11,709 tubes (corrected 11/04/2022)
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed to 43 states: AL, AZ, AR, CA, CO, CT, DE, FL, GA, HI, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MO, NE, NV, NH, NJ, NY, NC, ND, OH, OK, OR, PA, RI, SD, TN, TX, UT, VT, VA, WA, WI, DC
About Becton, Dickinson and Company, BD Biosciences
Becton, Dickinson and Company, BD Biosciences has 35 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report