FDA recall record

BD Biosciences, Systems & Reagents CD123 (9F5) PE Catalog number 649453 Analyte Specific recall — FDA Z-1375-2015

One lot of BD CD123 PE (ASR) has been determined to contain a low amount of CD4 antibody and may result in an unexpected staining pattern.

Class IIclassification
Z-1375-2015official record ID
Apr 8, 2015report date

Recall record at a glance

Official recordZ-1375-2015
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmBD Biosciences, Systems & Reagents
Report dateApr 8, 2015
Recall initiation dateMar 23, 2015
Quantity9
LocationSan Jose, CA, United States

Official product description

CD123 (9F5) PE Catalog number 649453 Analyte Specific Reagent

Why the product was recalled

One lot of BD CD123 PE (ASR) has been determined to contain a low amount of CD4 antibody and may result in an unexpected staining pattern.

Distribution information

US Distribution in states of: MO, GA, AZ, NE, TX, VA

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA 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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