FDA recall record

Diagnostic Hybrids MicroVue CIC-C1q EIA, Model A001 recall — FDA Z-1497-2018

A component of the kit was found to contain bacterial contamination.

Class IIIclassification
Z-1497-2018official record ID
May 2, 2018report date

Recall record at a glance

Official recordZ-1497-2018
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmDiagnostic Hybrids, Inc.
Report dateMay 2, 2018
Recall initiation dateNov 3, 2015
Quantity19 kits
LocationAthens, OH, United States

Official product description

MicroVue CIC-C1q EIA, Model A001. The MicroVue CIC-C1q EIA is for detection of circulating immune complexes (CIC) in human serum or plasma. The MicroVue CIC-C1q EIA is for detection of circulating immune complexes (CIC) in human serum or plasma. In certain disease states, immune complexes may initiate complement mediated damage of various organs and tissues. This activation of complement may begin a series of potentially destructive events including cell lysis, the production of anaphylatoxins, leukocyte stimulation and activation of macrophages. Major tissue damage can also occur when CIC fix to cell membranes as in some cases of glomerulonephritiscirculating immune complexes (CIC) in human serum or plasma.

Why the product was recalled

A component of the kit was found to contain bacterial contamination.

Distribution information

Worldwide Distribution - USA (nationwide) to the states of : CO, CT, IA, IL, MN, MO, NC, NY, OH TX, and UT., and to the countries of : Switzerland, India, Hong Kong, and Japan.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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