Becton Dickinson & Co. recalls Kit BD Max MRSA; Catalog # 442953

Recall date

July 17, 2019

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-2328-2019

FDA classification

Class II

Brand / firm

Becton Dickinson & Co.

Sold / distributed

AL, AR, AZ, CA, CO, CT, FL, GA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MT, NC, NH, NJ, NM, NV, NY, OH, OR, PA, PR, RI, SC, TN, TX, VA, WA, WI, WV Worldwide: Australia, Belgium, Brazil, Canada, Chile, China, Hong Kong, Japan, Korea, Mexico, Singapore, Taiwan

Why it was recalled

The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Kit BD Max MRSA; Catalog # 442953