Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
QIAGEN artus CMV RG PCR ASR (96) (Catalog number 4503225) Recalled by QIAGEN Gaithersburg, Inc. Due to CMV RG PCR kits may contain a mixture...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact QIAGEN Gaithersburg, Inc. directly.
Affected Products
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.
Quantity: 90 kits in total
Why Was This Recalled?
CMV RG PCR kits may contain a mixture of incorrect vials among the correct vials.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About QIAGEN Gaithersburg, Inc.
QIAGEN Gaithersburg, Inc. has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report