FDA recall record

BD Biosciences, Systems & Reagents BD Multi Check CD4 Low Control Catalog No. 340916 is recall — FDA Z-2233-2014

The outer box label contains the incorrect distribution date: Box states 2017-09-02 ; should be 2014-09-02

Class IIIclassification
Z-2233-2014official record ID
Aug 20, 2014report date

Recall record at a glance

Official recordZ-2233-2014
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmBD Biosciences, Systems & Reagents
Report dateAug 20, 2014
Recall initiation dateJul 18, 2014
Quantity85
LocationSan Jose, CA, United States

Official product description

BD Multi Check CD4 Low Control Catalog No. 340916 is intended as a complete process control for immunophenotyping by flow cytometry.

Why the product was recalled

The outer box label contains the incorrect distribution date: Box states 2017-09-02 ; should be 2014-09-02

Distribution information

IN, MA, TX, VA, Ca, KY, MD, PA, GA, and BD locations in Singapore and Belgium

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

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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