Diamedix Corporation recalls Diamedix Is-Mumps IgG Enzyme Immunoassay Test Kit for In Vitro Diagnostic Use Catalog No. 720-540

Recalled August 8, 2018 · FDA recall Z-2573-2018 · Diamedix

Hazard

Contains a gel-like contaminant that may affect product performance. · FDA Class III

Units

505

Sold at

AZ, CA, FL, IL, IN, KY, MA, MI, MN, MO, NH, NJ, NY, OH, OK, PA, RI, TN, TX, and WI

Description

Contains a gel-like contaminant that may affect product performance.

Product

Diamedix Is-Mumps IgG Enzyme Immunoassay Test Kit for In Vitro Diagnostic Use Catalog No. 720-540

Manufacturer(s)

Diamedix Corporation

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →