Cell Marque Corporation recalls H. pylori (polyclonal} 1.0 mL Catalog number 215A-76; Hematology - Analyte Specific Reagent In vitro diagnostic use - A…

Recall date

May 5, 2017

Source

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

Recall number

Z-2202-2017

FDA classification

Class II

Brand / firm

Cell Marque Corporation

Sold / distributed

Nationwide Distribution to CA, CO, DE, FL, GA, IL, KY, MD, MA, MS, NJ, NY, NC, OH, OK, OR, PA, TX.

Why it was recalled

Cell Marque has determined the need to issue a product recall after identifying product intended to be sold outside the U.S. was not properly labeled as "For Export Only" as required by section 801 (e )(1) of the FD&C Act.

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

What was recalled

H. pylori (polyclonal} 1.0 mL Catalog number 215A-76; Hematology - Analyte Specific Reagent In vitro diagnostic use - Analyte Specific Reagent