FDA recall record

Becton, Dickinson and Company, BD Biosciences BD Tritest CD3 FITC/CD4 PE/CD45 PerCP (IVD) recall — FDA Z-2378-2016

Internal review found that some vials of CD3/CD4/CD45 state that the product contains gelatin. The product does not contain gelatin and should state in…

Class IIIclassification
Z-2378-2016official record ID
Aug 17, 2016report date

Recall record at a glance

Official recordZ-2378-2016
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmBecton, Dickinson and Company, BD Biosciences
Report dateAug 17, 2016
Recall initiation dateJul 18, 2016
Quantity14,089
LocationSan Jose, CA, United States

Official product description

BD Tritest CD3 FITC/CD4 PE/CD45 PerCP (IVD); Catalog number 340383. Label states: Contains CD3 FITC/CD4 PE/CD45 per CP with Gelatin and 0.1% sodium azide. Hematology: BD Tritest CD3 fluorescein isothiocyanate (FITC)/CD4 phycoerythrin (PE)/CD45 peridinin chlorophyll protein (PerCP) is a three-color direct immunofluorescence reagent for use with a suitably equipped flow cytometer to identify and determine the percentages and absolute counts of mature human T lymphocytes (CD3+) and helper/inducer (CD3+CD4+) Tlymphocyte subsets in erythrocyte-lysed whole blood.

Why the product was recalled

Internal review found that some vials of CD3/CD4/CD45 state that the product contains gelatin. The product does not contain gelatin and should state in buffer.

Distribution information

Nationwide distribution to AR, CA, CO, IL, IN, LA, MA, MD, Ml, MN, NC, NJ, NM, NY, OR, PA, TN, TX, WA

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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About this record

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