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 (24) (Catalog number 4503223) 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 (24) (Catalog number 4503223) Product Usage: The artus CMV RG PCR ASR is designed to detect and to quantify nucleic acid specific to human cytomegalovirus (CMV) using real-time PCR technology (PCR) in the Rotor-Gene 2000/3000 (RG).
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