Home / Recalls / Medical Devices
QIAGEN Gaithersburg, Inc. recalls QIAGEN artus CMV RG PCR ASR (96) (Catalog number 4503225) Product Usage: Test is intended for use in the detection
Recalled May 22, 2013 · FDA recall Z-1320-2013 · QIAGEN Gaithersburg
Hazard
CMV RG PCR kits may contain a mixture of incorrect vials among the correct vials. · FDA Class II
Units
90 kits in total
Sold at
USA Nationwide Distribution including the states of: CA, DC, FL, GA, MA, MD, MI, and IL.
Description
CMV RG PCR kits may contain a mixture of incorrect vials among the correct vials.
Product
QIAGEN artus CMV RG PCR ASR (96) (Catalog number 4503225) Product Usage: Test is intended for use in the detection and quantitation of human cytomegalovirus (CMV) specific DNA, as part of an in house validated real-time PCR assay. One service package containing the handbook.
Manufacturer(s)
QIAGEN Gaithersburg, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →