FDA recall record

Becton Dickinson & Co BD BBL BCYE Selective Agar with PAV, Catalog # 297880, packaged in recall — FDA Z-1804-2013

Microbiological identification media may exhibit reduced levels of Vancomycin.

Class IIclassification
Z-1804-2013official record ID
Jul 31, 2013report date

Recall record at a glance

Official recordZ-1804-2013
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmBecton Dickinson & Co.
Report dateJul 31, 2013
Recall initiation dateJun 6, 2013
Quantity163 cartons
LocationSparks, MD, United States

Official product description

BD BBL BCYE Selective Agar with PAV, Catalog # 297880, packaged in cartons of 10 plates, and labeled in part ***Becton, Dickinson and Company 7 Loveton Circle Sparks, MD 21152 USA 800-638-8663 www.bd.com/ds*** BCYE Selective with PAV is used in qualitative procedures for isolation of Legionella species from clinical specimen and nonclinical (environmental) samples. It is similar to the Edelstein formula, except that the concentration of polymyxin B is reduced by half, and vancomycin is substituted for cefamandole.

Why the product was recalled

Microbiological identification media may exhibit reduced levels of Vancomycin.

Distribution information

Worldwide distribution: US (nationwide) and countries of:Belgium, Canada, Columbia, Mexico, Singapore, and Taiwan.

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

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About this record

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